U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C10H16O4S
Molecular Weight 232.297
Optical Activity ( + )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CAMPHORSULFONIC ACID, (+)-

SMILES

CC1(C)[C@@H]2CC[C@@]1(CS(O)(=O)=O)C(=O)C2

InChI

InChIKey=MIOPJNTWMNEORI-GMSGAONNSA-N
InChI=1S/C10H16O4S/c1-9(2)7-3-4-10(9,8(11)5-7)6-15(12,13)14/h7H,3-6H2,1-2H3,(H,12,13,14)/t7-,10-/m1/s1

HIDE SMILES / InChI

Approval Year

Unknown
139594
Name Type Language
CAMPHORSULFONIC ACID, (+)-
Common Name English
((1S,4R)-7,7-DIMETHYL-2-OXOBICYCLO(2.2.1)HEPT-1-YL)METHANESULFONIC ACID
Systematic Name English
REYCHLER'S ACID
Common Name English
D-CAMPHOR SULFONIC ACID
USP-RS  
Common Name English
CAMPHORSULFONIC ACID, D-
Common Name English
BICYCLO(2.2.1)HEPTANE-1-METHANESULFONIC ACID, 7,7-DIMETHYL-2-OXO-, (1S,4R)-
Systematic Name English
D-CAMPHORSULFONIC ACID
MI  
Common Name English
D-CAMPHOR SULFONIC ACID [USP-RS]
Common Name English
D-CAMPHORSULFONIC ACID [MI]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C851
Created by admin on Fri Dec 15 16:04:15 GMT 2023 , Edited by admin on Fri Dec 15 16:04:15 GMT 2023
Code System Code Type Description
NCI_THESAURUS
C77132
Created by admin on Fri Dec 15 16:04:15 GMT 2023 , Edited by admin on Fri Dec 15 16:04:15 GMT 2023
PRIMARY
MERCK INDEX
m3006
Created by admin on Fri Dec 15 16:04:15 GMT 2023 , Edited by admin on Fri Dec 15 16:04:15 GMT 2023
PRIMARY Merck Index
ECHA (EC/EINECS)
221-554-1
Created by admin on Fri Dec 15 16:04:15 GMT 2023 , Edited by admin on Fri Dec 15 16:04:15 GMT 2023
PRIMARY
CAS
3144-16-9
Created by admin on Fri Dec 15 16:04:15 GMT 2023 , Edited by admin on Fri Dec 15 16:04:15 GMT 2023
PRIMARY
WIKIPEDIA
CAMPHORSULFONIC ACID
Created by admin on Fri Dec 15 16:04:15 GMT 2023 , Edited by admin on Fri Dec 15 16:04:15 GMT 2023
PRIMARY
EPA CompTox
DTXSID00883956
Created by admin on Fri Dec 15 16:04:15 GMT 2023 , Edited by admin on Fri Dec 15 16:04:15 GMT 2023
PRIMARY
RS_ITEM_NUM
1087520
Created by admin on Fri Dec 15 16:04:15 GMT 2023 , Edited by admin on Fri Dec 15 16:04:15 GMT 2023
PRIMARY
FDA UNII
9TLZ01S15L
Created by admin on Fri Dec 15 16:04:15 GMT 2023 , Edited by admin on Fri Dec 15 16:04:15 GMT 2023
PRIMARY
SMS_ID
100000144027
Created by admin on Fri Dec 15 16:04:15 GMT 2023 , Edited by admin on Fri Dec 15 16:04:15 GMT 2023
PRIMARY
EVMPD
SUB127698
Created by admin on Fri Dec 15 16:04:15 GMT 2023 , Edited by admin on Fri Dec 15 16:04:15 GMT 2023
PRIMARY
CHEBI
55379
Created by admin on Fri Dec 15 16:04:15 GMT 2023 , Edited by admin on Fri Dec 15 16:04:15 GMT 2023
PRIMARY
EVMPD
SUB191204
Created by admin on Fri Dec 15 16:04:15 GMT 2023 , Edited by admin on Fri Dec 15 16:04:15 GMT 2023
ALTERNATIVE
EVMPD
SUB120778
Created by admin on Fri Dec 15 16:04:15 GMT 2023 , Edited by admin on Fri Dec 15 16:04:15 GMT 2023
PRIMARY
CHEBI
55403
Created by admin on Fri Dec 15 16:04:15 GMT 2023 , Edited by admin on Fri Dec 15 16:04:15 GMT 2023
PRIMARY
PUBCHEM
65617
Created by admin on Fri Dec 15 16:04:15 GMT 2023 , Edited by admin on Fri Dec 15 16:04:15 GMT 2023
PRIMARY
SALT/SOLVATE (PARENT)
Structure of AMOXYDRAMINE CAMSILATE
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
For language access assistance, contact the NCATS Public Information Officer
National Center for Advancing Translational Sciences (NCATS),
6701 Democracy Boulevard, Bethesda MD 20892-4874 • 301-594-8966