UCSF

ZINC00967520

Substance Information

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

Other Names:

(+)-2-Bornanone; (+)-Bornan-2-one; (+)-Camphor; (1R)-(+)-amphor; (1R)-Camphor; (1R,4R)-1,7,7-Trimethylbicyclo(2.2.1)heptan-2-one; (R)-(+)-Camphor; (R)-Camphor; AI3-01698; Alcanfor; Bicyclo(2.2.1)heptan-2-one, 1,7,7-trimethyl-, (1R)-; Bicyclo(2.2.1)heptan-

(+)-Bornan-2-one

(+)-bornan-2-one; (+)-camphor; (1R)-(+)-camphor; (R)-(+)-camphor; (R)-camphor; 464-49-3; CPD-862; D-camphor

(+)-bornan-2-one; (1R)-(+)-camphor; (1R,4R)-camphor; (R)-(+)-camphor; (R)-camphor; Camphor(D)

(+)-bornan-2-one;(+)-Camphor;(1R)-(+)-camphor;(1R,4R)-4,7,7-trimethylbicyclo[2.2.1]heptan-3-one;(1R,4R)-camphor;(R)-(+)-camphor;(R)-camphor;Camphor(D);D-Camphor;D-camphor

(+)-Camphor

(+)-Camphor; 464-49-3; C00808; d-Camphor

(+-)-Camphor; 1,7,7-Trimethylbicyclo(2.2.1)-2-heptanone; 1,7,7-Trimethylbicyclo(2.2.1)heptan-2-one; 1,7,7-Trimethylnorcamphor; 2-Bornanone; 2-Camphanone; 2-Kamfanon [Czech]; 2-Keto-1,7,7-trimethylnorcamphane; AI3-18783; Alphanon; BRN 1907611; BRN 3196099

(+/-)-Camphor

(+/-)-Camphor, 96%

(-)-Camphor

(-)-Camphor [464-48-2]

(-)-Camphor; 464-48-2; C00809

(-)-CAMPHOR; [464-48-2]

(1R)-(+)-Camphor

(1R)-(+)-Camphor, 98%

(1R,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one

(1R,4R)-4,7,7-trimethylbicyclo[2.2.1]heptan-3-one

(1S)-(-)-Camphor

(1S)-(-)-Camphor, 98%

(R)-camphor

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

2-bornanone; 2-camphanone; 2-keto-1,7,7-trimethylnorcamphane; Formosa camphor; Japan camphor; Kampfer; camphor; gum camphor; laurel camphor; root bark oil; spirit of camphor

738

76-22-2; C18369; Camphor; dl-Camphor

76-22-2; Camphor (USP); D00098; dl-Camphor (JP16)

8003-18-7; D05357; Parachlorophenol, camphorated (USAN)

Bicyclo(2.2.1)heptan-2-one, 1,7,7-trimethyl-, mixt. with 4-chlorophenol; C10H16O.C6H5ClO; LS-177527; Parachlorophenol, Camphorated; Parachlorophenol, Camphorated [USAN]; camphor paramonochlorophenol; camphorated monochlorophenol; camphorated monoparachlor

Bicyclo(2.2.1)heptan-2-one, 1,7,7-trimethyl-, mixt. with phenol; CCRIS 9228; Campho-phenique; Camphorated phenol; Carbol camphor; Carbolated camphor; LS-104185; Phenol, camphorated; Phenolated camphor

Bicyclo[2.2.1]hept-2-en-2-ol, 1,7,7-trimethyl-, (1R)- (9CI)

C10H16O; Camphor, (+-)-; Camphor, (+-)-Isomer; LS-48718

Camphor

Camphor (synthetic)

Camphor (synthetic), 96%+

Camphor (USP); D-Camphor (JAN); Dl-Camphor (JAN); Trans-Pi-Oxocamphor (JAN)

CHEBI:16; CHEBI:41334; CHEBI:10758; CHEBI:18442

D(+)-Camphor, 97%

D-(+)-Camphor

D-2-Bornanone

D-Camphor

DL-2-Bornanone

DL-Bornan-2-one

Dl-camphor

DL-Camphor, 96%

L(-)-Camphor, tech.

L-(-)-Camphor

L-2-Bornanone

LS-48720

MFCD00064148

MFCD00064149

MFCD00074738

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) 2.16 5.58 -4.65 0 1 0 17 152.237 0

Vendor Notes

Note Type Comments Provided By
Molecular_Solubility 2.413 Bitter DB
Melting_Point 172-176? Alfa-Aesar
Melting_Point 172-176° Alfa-Aesar
MP 174 TCI
Mp [°C] 175 - 177 Acros Organics
Melting_Point 175-180? Alfa-Aesar
Melting_Point 175-180° Alfa-Aesar
Mp [°C] 176 - 180 Acros Organics
MP 176-180 Oakwood Chemical
MP 177 TCI
MP 177-179 °C(lit.) Indofine
MP 178 TCI
Mp [°C] 178 - 180 Acros Organics
MP 178 - 182 Enamine Building Blocks
MP 178...182 Enamine Building Blocks
BP [°C] 204 Acros Organics
Boiling_Point 204? Alfa-Aesar
Boiling_Point 204° Alfa-Aesar
purity 9.500000000000000e+001 Enamine Building Blocks Enamine Building Blocks
Purity 95% Fluorochem
Therapy analgesic, antiinfective, antipruritic SMDC Iconix
UniProt Database Links CPXA_PSEPU; CRCB_ECOLI; FDEH_PSEPU; OTEMO_PSEPU; PAGP_ECOLI; PUTX_PSEPU; ZERSY_ZINZE ChEBI
Patent Database Links EP0893119; EP0989125; EP1106175; EP1158363; EP1167349; EP1449833; EP1495762; EP1495763; EP1506772; EP1514539; EP1514877; EP1552814; EP1600144; EP1602351; EP1602369; EP1621215; EP1632226; EP1639993; EP1647282; EP1661583; EP1666027; EP1685843; EP1698330; EP ChEBI
Hazard F: Highly flammable Acros Organics
Hazard F: Highly flammable; XI: Irritant Acros Organics
Hazard F: Highly flammable; XN: Harmful Acros Organics
H phrase H315: Causes skin irritation Acros Organics
H phrase H315: Causes skin irritation; H319: Causes serious eye irritation; H335: May cause respiratory irritation; H228: Flammable solid Acros Organics
H phrase H315: Causes skin irritation; H319: Causes serious eye irritation; H335: May cause respiratory irritation; H302: Harmful if swallowed; H228: Flammable solid Acros Organics
H phrase H315: Causes skin irritation; H335: May cause respiratory irritation; H319: Causes serious eye irritation; H228: Flammable solid Acros Organics
P phrase P261: Avoid breathing dust/fume/gas/mist/vapors/spray Acros Organics
P phrase P261: Avoid breathing dust/fume/gas/mist/vapors/spray; P302+ P352: IF ON SKIN: Wash with plenty of soap and water; P280: Wear protective gloves/protective clothing/eye protection/face protection; P305 + P351 + P338: IF IN EYES: Rinse cautiously with water Acros Organics
R phrase R11: Highly flammable. Acros Organics
R phrase R11: Highly flammable.; R22: Harmful if swallowed.; R36/37/38: Irritating to eyes, respiratory system and skin. Acros Organics
R phrase R11: Highly flammable.; R36/37/38: Irritating to eyes, respiratory system and skin. Acros Organics
Reactome Database Links REACT_15538; REACT_163726; REACT_22239; REACT_22289 ChEBI
S phrase S16: Keep away from sources of ignition - No smoking. Acros Organics
S phrase S16: Keep away from sources of ignition - No smoking.; S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.; S37/39: Wear suitable gloves and eye/face protection. Acros Organics
PUBCHEM_PATENT_ID US4250108 IBM Patent Data

Activity (Go SEA)

Direct Reactome Annotations (via ChEBI)

Description Species
Class C/3 (Metabotropic glutamate/pheromone receptors)
G alpha (i) signalling events

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