NP-MRD: Showing NP-Card for 1-chloro-n-{2-chloro-2-[(1z,3r,4s,5s)-4-chloro-5-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexylidene]ethyl}methanecarbonimidoyl chloride (NP0196516)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-04 14:37:20 UTC

Updated at

2022-09-04 14:37:20 UTC

NP-MRD ID

NP0196516

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-chloro-n-{2-chloro-2-[(1z,3r,4s,5s)-4-chloro-5-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexylidene]ethyl}methanecarbonimidoyl chloride

Description

1-Chloro-N-{2-chloro-2-[(1Z,3R,4S,5S)-4-chloro-5-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexylidene]ethyl}methanecarbonimidoyl chloride belongs to the class of organic compounds known as isocyanide dichlorides. These are organonitrogen compounds derived from isocyanide, with the general formula RN=C(Cl)Cl (R = organyl). 1-chloro-n-{2-chloro-2-[(1z,3r,4s,5s)-4-chloro-5-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexylidene]ethyl}methanecarbonimidoyl chloride is found in Reticulidia fungia. Based on a literature review very few articles have been published on 1-chloro-N-{2-chloro-2-[(1Z,3R,4S,5S)-4-chloro-5-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexylidene]ethyl}methanecarbonimidoyl chloride.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 45 45  0  0  0  0  0  0  0  0999 V2000
    4.1798    0.0001   -1.2829 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1315    0.4664    0.1122 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4747    1.0042    0.6170 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1591    0.4914    0.9602 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7500    0.0856    0.8978 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3184   -0.3580   -0.4335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1395   -0.8155   -0.4753 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4187   -1.2372   -1.9001 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0517    0.3317   -0.1341 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4475   -0.1575   -0.1565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4545    0.7023   -0.0442 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1277    0.1579   -0.0673 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -3.1506    2.1416    0.1085 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6891    2.6364    1.3428 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2257    3.7851    1.3629 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8858    4.4040    2.8531 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -4.3058    4.7416   -0.0832 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -2.7333   -1.5858   -0.2973 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7691   -2.5103    0.3834 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2452   -2.8062    1.6809 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3635   -2.0102    0.4104 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7445   -3.2958   -0.1211 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    3.4166    0.3603   -1.9579 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1643    0.3064   -1.7799 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2243   -1.1219   -1.2463 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6724    1.9911    0.1544 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2675    0.3187    0.2635 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5055    1.0419    1.7036 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4347    0.9162    1.9856 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6445   -0.7873    1.6254 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1449    0.9390    1.3038 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3128    0.5269   -1.1460 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9245   -1.1462   -0.8523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2062   -0.5908   -2.3520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6831   -2.3327   -1.9641 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5155   -1.1683   -2.5130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8153    0.8092    0.8418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9394    1.0782   -0.9732 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6176    2.6775   -0.7507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0651    2.3185    0.1553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9492   -1.8902   -1.3656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7363   -1.7731    0.1995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7997   -3.4770   -0.1606 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0547   -3.3626    1.6143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1113   -1.8060    1.4809 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  7  6  1  6
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  2  3
 15 16  1  0
 15 17  1  0
 21  7  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  3 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  0
  6 33  1  0
  8 34  1  0
  8 35  1  0
  8 36  1  0
  9 37  1  0
  9 38  1  0
 18 41  1  0
 18 42  1  0
 19 43  1  6
 20 44  1  0
 21 45  1  1
 13 39  1  0
 13 40  1  0
M  END


  Mrv1652309042216372D          

 22 22  0  0  1  0            999 V2000
    1.4929    3.2767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3054    3.1335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8357    3.7654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5875    2.3582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0572    1.7262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2448    1.8695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1842    1.8695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  6  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 10 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
  7 21  1  0  0  0  0
 21 22  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0196516

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC[C@]1(C)C\C(C[C@H](O)[C@H]1Cl)=C(\Cl)CN=C(Cl)Cl

> <INCHI_IDENTIFIER>
InChI=1S/C16H23Cl4NO/c1-10(2)5-4-6-16(3)8-11(7-13(22)14(16)18)12(17)9-21-15(19)20/h5,13-14,22H,4,6-9H2,1-3H3/b12-11+/t13-,14+,16+/m0/s1

> <INCHI_KEY>
NWMWDIMFPYWPMI-RVLRRZAOSA-N

> <FORMULA>
C16H23Cl4NO

> <MOLECULAR_WEIGHT>
387.17

> <EXACT_MASS>
385.0533752

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
39.432206172827335

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-chloro-N-{2-chloro-2-[(1Z,3R,4S,5S)-4-chloro-5-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexylidene]ethyl}methanecarbonimidoyl chloride

> <JCHEM_LOGP>
5.316695189

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.033257719756403

> <JCHEM_PKA_STRONGEST_BASIC>
-0.13687886098193702

> <JCHEM_POLAR_SURFACE_AREA>
32.59

> <JCHEM_REFRACTIVITY>
98.75850000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
1-chloro-N-{2-chloro-2-[(1Z,3R,4S,5S)-4-chloro-5-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexylidene]ethyl}methanecarbonimidoyl chloride

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       2.787   6.117   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.303   5.849   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.293   7.029   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.830   4.402   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.840   3.222   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.324   3.490   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.344   3.490   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   12 Cl   UNK     0       4.001  -2.310   0.000  0.00  0.00          Cl+0
HETATM   13  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0       5.335   1.540   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   16 Cl   UNK     0       6.668   3.850   0.000  0.00  0.00          Cl+0
HETATM   17 Cl   UNK     0       8.002   1.540   0.000  0.00  0.00          Cl+0
HETATM   18  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   22 Cl   UNK     0      -1.334   2.310   0.000  0.00  0.00          Cl+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9   21                                             
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   18                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   10   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19    7   22                                                  
CONECT   22   21                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   44    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₂₃Cl₄NO

Average Mass

387.1700 Da

Monoisotopic Mass

385.05338 Da

IUPAC Name

1-chloro-N-{2-chloro-2-[(1Z,3R,4S,5S)-4-chloro-5-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexylidene]ethyl}methanecarbonimidoyl chloride

Traditional Name

1-chloro-N-{2-chloro-2-[(1Z,3R,4S,5S)-4-chloro-5-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexylidene]ethyl}methanecarbonimidoyl chloride

CAS Registry Number

Not Available

SMILES

CC(C)=CCC[C@]1(C)C\C(C[C@H](O)[C@H]1Cl)=C(\Cl)CN=C(Cl)Cl

InChI Identifier

InChI=1S/C16H23Cl4NO/c1-10(2)5-4-6-16(3)8-11(7-13(22)14(16)18)12(17)9-21-15(19)20/h5,13-14,22H,4,6-9H2,1-3H3/b12-11+/t13-,14+,16+/m0/s1

InChI Key

NWMWDIMFPYWPMI-RVLRRZAOSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Reticulidia fungia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as isocyanide dichlorides. These are organonitrogen compounds derived from isocyanide, with the general formula RN=C(Cl)Cl (R = organyl).

Kingdom

Organic compounds

Super Class

Organic nitrogen compounds

Class

Organonitrogen compounds

Sub Class

Isocyanide dichlorides

Direct Parent

Isocyanide dichlorides

Alternative Parents

Substituents

Cyclic alcohol
Isocyanide dichloride
Chlorohydrin
Halohydrin
Secondary alcohol
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Vinyl halide
Vinyl chloride
Haloalkene
Chloroalkene
Organopnictogen compound
Alkyl chloride
Organooxygen compound
Organochloride
Organohalogen compound
Organic oxygen compound
Alcohol
Alkyl halide
Hydrocarbon derivative
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	5.32	ChemAxon
pKa (Strongest Acidic)	14.03	ChemAxon
pKa (Strongest Basic)	-0.14	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	32.59 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	98.76 m³·mol⁻¹	ChemAxon
Polarizability	39.43 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

10470103

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

23425016

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-chloro-n-{2-chloro-2-[(1z,3r,4s,5s)-4-chloro-5-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexylidene]ethyl}methanecarbonimidoyl chloride (NP0196516)

MOL for NP0196516 (1-chloro-n-{2-chloro-2-[(1z,3r,4s,5s)-4-chloro-5-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexylidene]ethyl}methanecarbonimidoyl chloride)

3D MOL for NP0196516 (1-chloro-n-{2-chloro-2-[(1z,3r,4s,5s)-4-chloro-5-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexylidene]ethyl}methanecarbonimidoyl chloride)

3D SDF for NP0196516 (1-chloro-n-{2-chloro-2-[(1z,3r,4s,5s)-4-chloro-5-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexylidene]ethyl}methanecarbonimidoyl chloride)

3D-SDF for NP0196516 (1-chloro-n-{2-chloro-2-[(1z,3r,4s,5s)-4-chloro-5-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexylidene]ethyl}methanecarbonimidoyl chloride)

PDB for NP0196516 (1-chloro-n-{2-chloro-2-[(1z,3r,4s,5s)-4-chloro-5-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexylidene]ethyl}methanecarbonimidoyl chloride)

3D PDB for NP0196516 (1-chloro-n-{2-chloro-2-[(1z,3r,4s,5s)-4-chloro-5-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexylidene]ethyl}methanecarbonimidoyl chloride)

SMILES for NP0196516 (1-chloro-n-{2-chloro-2-[(1z,3r,4s,5s)-4-chloro-5-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexylidene]ethyl}methanecarbonimidoyl chloride)

INCHI for NP0196516 (1-chloro-n-{2-chloro-2-[(1z,3r,4s,5s)-4-chloro-5-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexylidene]ethyl}methanecarbonimidoyl chloride)

Structure for NP0196516 (1-chloro-n-{2-chloro-2-[(1z,3r,4s,5s)-4-chloro-5-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexylidene]ethyl}methanecarbonimidoyl chloride)

3D Structure for NP0196516 (1-chloro-n-{2-chloro-2-[(1z,3r,4s,5s)-4-chloro-5-hydroxy-3-methyl-3-(4-methylpent-3-en-1-yl)cyclohexylidene]ethyl}methanecarbonimidoyl chloride)