NP-MRD: Showing NP-Card for 1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl formate (NP0243654)

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Record Information

Version

2.0

Created at

2022-09-07 04:15:12 UTC

Updated at

2022-09-07 04:15:13 UTC

NP-MRD ID

NP0243654

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl formate

Description

Bornyl formate, also known as bornyl methanoate or fema 2161, belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other. Bornyl formate is an extremely weak basic (essentially neutral) compound (based on its pKa). Bornyl formate is a camphor, earth, and green tasting compound. 1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl formate is found in Ageratum conyzoides and Valeriana officinalis. Outside of the human body,.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 31 32  0  0  0  0  0  0  0  0999 V2000
   -0.9214    1.5465   -0.9203 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0202    0.2710   -0.1662 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2801   -0.4695   -0.5025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8865    0.5016    1.3489 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8925   -0.9103    1.8470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0639   -1.6411    0.7801 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2204   -0.5990   -0.2960 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4634   -1.1407   -1.6277 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2801    0.2985    0.2676 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8153    1.2005   -0.6423 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1805    1.1847   -0.8904 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8880    0.3475   -0.2774 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5434    1.0000    1.4121 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4060    2.3580   -0.3905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9687    1.9155   -1.0989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4349    1.4480   -1.9109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1812   -1.5655   -0.4217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4976   -0.2670   -1.5850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1520   -0.0738    0.0542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6252    1.1633    1.7517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8816   -1.3693    1.8923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3691   -0.9608    2.8247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5738   -2.5222    0.3922 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9187   -1.9130    1.2376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2815   -0.8045   -2.3962 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5007   -0.9813   -1.9578 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3322   -2.2636   -1.5969 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0561   -0.3738    0.7201 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6597    1.8618   -1.5883 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9489    0.6702    2.3939 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6289    2.0880    1.3468 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  6
  7  9  1  0
  9 13  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
  7  2  1  0
 13  4  1  0
  1 14  1  0
  1 15  1  0
  1 16  1  0
  3 17  1  0
  3 18  1  0
  3 19  1  0
  4 20  1  1
  5 21  1  0
  5 22  1  0
  6 23  1  0
  6 24  1  0
  8 25  1  0
  8 26  1  0
  8 27  1  0
  9 28  1  1
 13 30  1  0
 13 31  1  0
 11 29  1  0
M  END

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      -1.428   3.154   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.284   1.796   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.071   2.296   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.213  -0.987   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.284   0.296   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.213   1.298   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.072   2.796   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.215   2.152   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.071   1.011   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.215  -0.204   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       1.713  -1.630   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       1.128  -2.308   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       1.422  -3.154   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    5    8                                             
CONECT    3    2                                                            
CONECT    4    5                                                            
CONECT    5    2    4    6   10                                             
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    2    7    9                                                  
CONECT    9    8   10                                                       
CONECT   10    5    9   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12                                                            
MASTER        0    0    0    0    0    0    0    0   13    0   28    0
END

View in JSmol

Synonyms

Value	Source
Bornyl formic acid	Generator
1,7,7-Trimethyl-formateendo-bicyclo(2.2.1)heptan-2-ol	HMDB
1,7,7-Trimethyl-formateendo-bicyclo[2.2.1]heptan-2-ol	HMDB
2-Camphanyl formate	HMDB
Borneol, formate	HMDB
Bornyl methanoate	HMDB
endo-1,7,7-Trimethylbicyclo(2.2.1)hept-2-yl formate	HMDB
endo-1,7,7-Trimethylbicyclo(2.2.1)heptan-2-yl formate	HMDB
endo-2-Bornanyl formate	HMDB
Endoisobornylformate	HMDB
FEMA 2161	HMDB
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl formic acid	Generator
Isobornyl formic acid	Generator

Chemical Formula

C₁₁H₁₈O₂

Average Mass

182.2594 Da

Monoisotopic Mass

182.13068 Da

IUPAC Name

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl formate

Traditional Name

1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl formate

CAS Registry Number

Not Available

SMILES

CC1(C)C2CCC1(C)C(C2)OC=O

InChI Identifier

InChI=1S/C11H18O2/c1-10(2)8-4-5-11(10,3)9(6-8)13-7-12/h7-9H,4-6H2,1-3H3

InChI Key

RDWUNORUTVEHJF-UHFFFAOYSA-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
Ageratum conyzoides	LOTUS Database	35616633
Valeriana officinalis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Bicyclic monoterpenoids

Alternative Parents

Substituents

Bicyclic monoterpenoid
Bornane monoterpenoid
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	3.34	ALOGPS
logP	2.38	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Basic)	-6.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	26.3 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	49.98 m³·mol⁻¹	ChemAxon
Polarizability	20.62 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0038245

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB017541

KNApSAcK ID

Not Available

Chemspider ID

452382

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

518472

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl formate (NP0243654)

MOL for NP0243654 (1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl formate)

3D MOL for NP0243654 (1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl formate)

3D SDF for NP0243654 (1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl formate)

3D-SDF for NP0243654 (1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl formate)

PDB for NP0243654 (1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl formate)

3D PDB for NP0243654 (1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl formate)

SMILES for NP0243654 (1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl formate)

INCHI for NP0243654 (1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl formate)

Structure for NP0243654 (1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl formate)

3D Structure for NP0243654 (1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl formate)