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Details

Stereochemistry RACEMIC
Molecular Formula C10H12ClNO4
Molecular Weight 245.66
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CHLORPHENESIN CARBAMATE

SMILES

NC(=O)OCC(O)COC1=CC=C(Cl)C=C1

InChI

InChIKey=SKPLBLUECSEIFO-UHFFFAOYSA-N
InChI=1S/C10H12ClNO4/c11-7-1-3-9(4-2-7)15-5-8(13)6-16-10(12)14/h1-4,8,13H,5-6H2,(H2,12,14)

HIDE SMILES / InChI

Molecular Formula C10H12ClNO4
Molecular Weight 245.66
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:08:39 UTC 2023
Edited
by admin
on Fri Dec 15 16:08:39 UTC 2023
Record UNII
57U5YI11WP
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CHLORPHENESIN CARBAMATE
GREEN BOOK   HSDB   MART.   MI   ORANGE BOOK   USAN   VANDF   WHO-DD  
USAN  
Official Name English
CHLORPHENESIN CARBAMATE [GREEN BOOK]
Common Name English
CHLORPHENESIN CARBAMATE [JAN]
Common Name English
CHLORPHENESIN CARBAMATE [ORANGE BOOK]
Common Name English
CHLORPHENESIN CARBAMATE [USAN]
Common Name English
Chlorphenesin carbamate [WHO-DD]
Common Name English
MAOLATE
Brand Name English
U-19646
Code English
1,2-PROPANEDIOL, 3-(4-CHLOROPHENOXY)-, 1-CARBAMATE
Common Name English
CHLORPHENESIN CARBAMATE [HSDB]
Common Name English
CHLORPHENESIN CARBAMATE [VANDF]
Common Name English
NSC-82943
Code English
3-(P-CHLOROPHENOXY)-1,2-PROPANEDIOL 1-CARBAMATE
Common Name English
U-19,646
Code English
CHLORPHENESIN CARBAMATE [MI]
Common Name English
CHLORPHENESIN CARBAMATE [MART.]
Common Name English
Classification Tree Code System Code
CFR 21 CFR 520.434
Created by admin on Fri Dec 15 16:08:40 UTC 2023 , Edited by admin on Fri Dec 15 16:08:40 UTC 2023
NCI_THESAURUS C29578
Created by admin on Fri Dec 15 16:08:40 UTC 2023 , Edited by admin on Fri Dec 15 16:08:40 UTC 2023
Code System Code Type Description
PUBCHEM
2724
Created by admin on Fri Dec 15 16:08:40 UTC 2023 , Edited by admin on Fri Dec 15 16:08:40 UTC 2023
PRIMARY
NCI_THESAURUS
C65322
Created by admin on Fri Dec 15 16:08:40 UTC 2023 , Edited by admin on Fri Dec 15 16:08:40 UTC 2023
PRIMARY
MERCK INDEX
m3455
Created by admin on Fri Dec 15 16:08:40 UTC 2023 , Edited by admin on Fri Dec 15 16:08:40 UTC 2023
PRIMARY Merck Index
CAS
886-74-8
Created by admin on Fri Dec 15 16:08:40 UTC 2023 , Edited by admin on Fri Dec 15 16:08:40 UTC 2023
PRIMARY
WIKIPEDIA
Chlorphenesin carbamate
Created by admin on Fri Dec 15 16:08:40 UTC 2023 , Edited by admin on Fri Dec 15 16:08:40 UTC 2023
PRIMARY
RXCUI
20880
Created by admin on Fri Dec 15 16:08:40 UTC 2023 , Edited by admin on Fri Dec 15 16:08:40 UTC 2023
PRIMARY RxNorm
MESH
C015071
Created by admin on Fri Dec 15 16:08:40 UTC 2023 , Edited by admin on Fri Dec 15 16:08:40 UTC 2023
PRIMARY
EPA CompTox
DTXSID5022803
Created by admin on Fri Dec 15 16:08:40 UTC 2023 , Edited by admin on Fri Dec 15 16:08:40 UTC 2023
PRIMARY
NSC
82943
Created by admin on Fri Dec 15 16:08:40 UTC 2023 , Edited by admin on Fri Dec 15 16:08:40 UTC 2023
PRIMARY
DAILYMED
57U5YI11WP
Created by admin on Fri Dec 15 16:08:40 UTC 2023 , Edited by admin on Fri Dec 15 16:08:40 UTC 2023
PRIMARY
CHEBI
3643
Created by admin on Fri Dec 15 16:08:40 UTC 2023 , Edited by admin on Fri Dec 15 16:08:40 UTC 2023
PRIMARY
EVMPD
SUB01245MIG
Created by admin on Fri Dec 15 16:08:40 UTC 2023 , Edited by admin on Fri Dec 15 16:08:40 UTC 2023
PRIMARY
ECHA (EC/EINECS)
212-954-7
Created by admin on Fri Dec 15 16:08:40 UTC 2023 , Edited by admin on Fri Dec 15 16:08:40 UTC 2023
PRIMARY
FDA UNII
57U5YI11WP
Created by admin on Fri Dec 15 16:08:40 UTC 2023 , Edited by admin on Fri Dec 15 16:08:40 UTC 2023
PRIMARY
DRUG CENTRAL
614
Created by admin on Fri Dec 15 16:08:40 UTC 2023 , Edited by admin on Fri Dec 15 16:08:40 UTC 2023
PRIMARY
SMS_ID
100000084718
Created by admin on Fri Dec 15 16:08:40 UTC 2023 , Edited by admin on Fri Dec 15 16:08:40 UTC 2023
PRIMARY
HSDB
3031
Created by admin on Fri Dec 15 16:08:40 UTC 2023 , Edited by admin on Fri Dec 15 16:08:40 UTC 2023
PRIMARY
ChEMBL
CHEMBL607710
Created by admin on Fri Dec 15 16:08:40 UTC 2023 , Edited by admin on Fri Dec 15 16:08:40 UTC 2023
PRIMARY
DRUG BANK
DB14656
Created by admin on Fri Dec 15 16:08:40 UTC 2023 , Edited by admin on Fri Dec 15 16:08:40 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY