UCSF

ZINC00967533

Draw Identity 99% 90% 80% 70%

Substance Information

In ZINC since Heavy atoms Benign functionality
August 6th, 2004 11 Yes

Popular Name: Borneol Borneol

Find On: PubMed — Wikipedia — Google

CAS Numbers: 124-76-5 , 464-43-7 , 464-45-9 , 507-70-0 , 791787-82-1 , [124-76-5] , [464-45-9]

Other Names:

"(-)-Borneol, 97%"

(+)-Borneol

(+)-Borneol; (1R,2S,4R)-Borneol; (1R-endo)-1,7,7-Trimethylbicyclo(2.2.1)heptan-2-ol; BRN 2038056; Bicyclo(2.2.1)heptan-2-ol, 1,7,7-trimethyl-, (1R-endo)-; CCRIS 6550; D-Borneol; EINECS 207-352-6; LS-45113

(+/-)-Borneol

(+/-)-Isoborneol

(-)-Borneol

(-)-Borneol, 97+%

(-)-Borneol, 98%

(-)-Borneol; (1S,2R,4S)-(-)-Borneol; 464-45-9; C01766; L-Borneol; Linderol

(-)-borneol; (1S,2R,4S)-(-)-borneol; CPD-1908; L-borneol

(1S,2R,4S)-(-)-borneol; (1S,2R,4S)-borneol; (1S-endo)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol; L-borneol; l-borneol

(1S,2R,4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol

(?)-Isoborneol, 95%

(ñ)-Isoborneol, 95%

(±)-Isoborneol

(±)-Isoborneol, 95%

1,7,7-Trimethyl-(1R,2S,4R)-rel-Bicyclo[2.2.1]heptan-2-ol;1,7,7-Trimethyl-endo-Bicyclo[2.2.1]heptan-2-ol;Borneo camphor;Borneol;Borneol (8CI);Bornyl alcohol;Dl-Borneol;Endo-(-)-Bornan-2-ol;Endo-2-bornanol;Endo-2-camphanol;Endo-2-Hydroxy-1,7,7-trimethylnorb

1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol

507-70-0; Borneol; C01411

Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, (1S,4S)- (9CI)

Borneo camphor; Sumatra camphor; bornyl alcohol; endo-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol; endo-2-bornanol; endo-2-camphanol; endo-2-hydroxycamphane

CHEBI:3150; CHEBI:22913

CHEBI:83; CHEBI:18478; CHEBI:10773

DL-Isoborneol

DL-Isoborneol, 93%, tech.

exo-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol

L(-)-Borneol

L(-)-Borneol, 97%

MFCD00003759

MFCD00064162

MFCD00066426

MFCD00074821

[(1s)-endo]-(−)-borneol

Download: MOL2 SDF SMILES Flexibase

Annotations

Vendors

Physical Representations

Type pH range xlogP Des A‑Pol Apolar desolvation (kcal/mol) Des Pol Polar desolvation (kcal/mol) H Don H-bond donors H Acc H-bond acceptors Chg Net charge tPSA (Ų) MWT Molecular weight (g/mol) RB Rotatable bonds DL
Ref Reference (pH 7) 2.35 3.28 -1.98 1 1 0 20 154.253 0 ↓

Vendor Notes

Note Type Comments Provided By
Mp [°C] 204 - 208 Acros Organics
MP 206 TCI
Mp [°C] 208 - 214 Acros Organics
Melting_Point 208-211? Alfa-Aesar
Melting_Point 208-211° Alfa-Aesar
BP [°C] 210 Acros Organics
Boiling_Point 210? Alfa-Aesar
Boiling_Point 210° Alfa-Aesar
MP 211 TCI
purity 9.500000000000000e+001 Enamine Building Blocks Enamine Building Blocks
Melting_Point ca 210? subl. Alfa-Aesar
Melting_Point ca 210° subl. Alfa-Aesar
PUBCHEM_PATENT_ID EP0054431A1; EP0121284A2; EP0121284B1; EP0173142A2; EP0232742A1; EP0351382B1; EP0414200A2; EP0414200B1; EP0427168A1; EP0427168B1; EP0458363B1; EP0458643A2; EP0458643B1; EP0605637A1; EP0605637B1; EP0619141A1; EP0658533A1; EP0658533B1; EP0884314A2; EP101934 IBM Patent Data
Patent Database Links EP1506782; EP1514877; EP1552814; EP1666027; EP1679058; EP1700595; EP1741439; EP1762215; US2005256069; US2007184133; US2007224261; US2007225364; WO2007095156; WO2008116321 ChEBI
Hazard F: Highly flammable Acros Organics
H phrase H228: Flammable solid Acros Organics
P phrase P210: Keep away from heat/sparks/open flames/hot surfaces. - No smoking Acros Organics
R phrase R11: Highly flammable. Acros Organics
S phrase S16: Keep away from sources of ignition - No smoking. Acros Organics
S phrase S24/25: Avoid contact with skin and eyes. Acros Organics
UniProt Database Links UD2A1_HUMAN; UDB15_RAT; ZERSY_ZINZE ChEBI
UniProt Database Links UDB15_RAT ChEBI
PUBCHEM_PATENT_ID US6146806 IBM Patent Data

Activity (Go SEA)

Analogs ( Draw Identity 99% 90% 80% 70% )