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Examples:
iron*
,
InChI=1S/CH4O/c1-2/h2H,1H3
,
caffeine
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ChEBI
> Main
CHEBI:15397 - (
S
)-camphor
Main
ChEBI Ontology
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ChEBI Name
(
S
)-camphor
ChEBI ID
CHEBI:15397
ChEBI ASCII Name
(S)-camphor
Definition
The
S
-enantiomer of camphor.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:85, CHEBI:10774, CHEBI:18479
Supplier Information
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Molfile
Molfile
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Formula
C10H16O
Net Charge
0
Average Mass
152.23344
Monoisotopic Mass
152.12012
InChI
InChI=1S/C10H16O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7H,4-6H2,1-3H3/t7-,10+/m0/s1
InChIKey
DSSYKIVIOFKYAU-OIBJUYFYSA-N
SMILES
CC1(C)[C@H]2CC[C@]1(C)C(=O)C2
Roles Classification
Biological Role
(s):
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
(via
camphor
)
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
(
S
)-camphor (
CHEBI:15397
)
is a
camphor (
CHEBI:36773
)
(
S
)-camphor (
CHEBI:15397
)
is enantiomer of
(
R
)-camphor (
CHEBI:15396
)
Incoming
(
R
)-camphor (
CHEBI:15396
)
is enantiomer of
(
S
)-camphor (
CHEBI:15397
)
IUPAC Name
(1
S
,4
S
)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
Synonyms
Sources
(−)-bornan-2-one
ChemIDplus
(−)-camphor
NIST Chemistry WebBook
(-)-Camphor
KEGG COMPOUND
(1
S
)-(−)-camphor
NIST Chemistry WebBook
(1
S
,4
S
)-camphor
UniProt
l
-camphor
ChemIDplus
Manual Xref
Database
C00809
KEGG COMPOUND
View more database links
Registry Numbers
Types
Sources
1907612
Reaxys Registry Number
Reaxys
1907612
Beilstein Registry Number
Beilstein
4291747
Beilstein Registry Number
Beilstein
464-48-2
CAS Registry Number
KEGG COMPOUND
464-48-2
CAS Registry Number
NIST Chemistry WebBook
464-48-2
CAS Registry Number
ChemIDplus
874917
Gmelin Registry Number
Gmelin
Last Modified
13 November 2017