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

Details

Stereochemistry ACHIRAL
Molecular Formula C2H7AsO2
Molecular Weight 137.9974
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CACODYLIC ACID

SMILES

C[As](C)(O)=O

InChI

InChIKey=OGGXGZAMXPVRFZ-UHFFFAOYSA-N
InChI=1S/C2H7AsO2/c1-3(2,4)5/h1-2H3,(H,4,5)

HIDE SMILES / InChI

Approval Year

Name Type Language
CACODYLIC ACID
MI   WHO-DD  
Systematic Name English
HYDROXYDIMETHYLARSINE OXIDE
Systematic Name English
DIMETHYLARSINIC ACID
Systematic Name English
DIMETHYLARSINIC ACID [IARC]
Common Name English
NSC-103115
Code English
Cacodylic acid [WHO-DD]
Common Name English
DIMETHYLARSENIC ACID [HSDB]
Common Name English
CACODYLIC ACID [MI]
Common Name English
Classification Tree Code System Code
IARC Dimethylarsinic acid
NCI_THESAURUS C737
Created by admin on Fri Dec 15 14:58:45 UTC 2023 , Edited by admin on Fri Dec 15 14:58:45 UTC 2023
EPA PESTICIDE CODE 12501
Created by admin on Fri Dec 15 14:58:45 UTC 2023 , Edited by admin on Fri Dec 15 14:58:45 UTC 2023
Code System Code Type Description
DRUG CENTRAL
3058
Created by admin on Fri Dec 15 14:58:45 UTC 2023 , Edited by admin on Fri Dec 15 14:58:45 UTC 2023
PRIMARY
CHEBI
48765
Created by admin on Fri Dec 15 14:58:45 UTC 2023 , Edited by admin on Fri Dec 15 14:58:45 UTC 2023
PRIMARY
SMS_ID
100000182554
Created by admin on Fri Dec 15 14:58:45 UTC 2023 , Edited by admin on Fri Dec 15 14:58:45 UTC 2023
PRIMARY
ECHA (EC/EINECS)
200-883-4
Created by admin on Fri Dec 15 14:58:45 UTC 2023 , Edited by admin on Fri Dec 15 14:58:45 UTC 2023
PRIMARY
PUBCHEM
2513
Created by admin on Fri Dec 15 14:58:45 UTC 2023 , Edited by admin on Fri Dec 15 14:58:45 UTC 2023
PRIMARY
ALANWOOD
cacodylic acid
Created by admin on Fri Dec 15 14:58:45 UTC 2023 , Edited by admin on Fri Dec 15 14:58:45 UTC 2023
PRIMARY
MESH
D002101
Created by admin on Fri Dec 15 14:58:45 UTC 2023 , Edited by admin on Fri Dec 15 14:58:45 UTC 2023
PRIMARY
EVMPD
SUB196704
Created by admin on Fri Dec 15 14:58:45 UTC 2023 , Edited by admin on Fri Dec 15 14:58:45 UTC 2023
PRIMARY
NSC
103115
Created by admin on Fri Dec 15 14:58:45 UTC 2023 , Edited by admin on Fri Dec 15 14:58:45 UTC 2023
PRIMARY
MERCK INDEX
m2879
Created by admin on Fri Dec 15 14:58:45 UTC 2023 , Edited by admin on Fri Dec 15 14:58:45 UTC 2023
PRIMARY Merck Index
HSDB
360
Created by admin on Fri Dec 15 14:58:45 UTC 2023 , Edited by admin on Fri Dec 15 14:58:45 UTC 2023
PRIMARY
NCI_THESAURUS
C80595
Created by admin on Fri Dec 15 14:58:45 UTC 2023 , Edited by admin on Fri Dec 15 14:58:45 UTC 2023
PRIMARY
CAS
75-60-5
Created by admin on Fri Dec 15 14:58:45 UTC 2023 , Edited by admin on Fri Dec 15 14:58:45 UTC 2023
PRIMARY
EPA CompTox
DTXSID7020508
Created by admin on Fri Dec 15 14:58:45 UTC 2023 , Edited by admin on Fri Dec 15 14:58:45 UTC 2023
PRIMARY
WIKIPEDIA
CACODYLIC ACID
Created by admin on Fri Dec 15 14:58:45 UTC 2023 , Edited by admin on Fri Dec 15 14:58:45 UTC 2023
PRIMARY
FDA UNII
AJ2HL7EU8K
Created by admin on Fri Dec 15 14:58:45 UTC 2023 , Edited by admin on Fri Dec 15 14:58:45 UTC 2023
PRIMARY
DRUG BANK
DB02994
Created by admin on Fri Dec 15 14:58:45 UTC 2023 , Edited by admin on Fri Dec 15 14:58:45 UTC 2023
PRIMARY