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Details

Stereochemistry RACEMIC
Molecular Formula C13H21N3O3.ClH
Molecular Weight 303.785
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CARBUTEROL HYDROCHLORIDE

SMILES

Cl.CC(C)(C)NCC(O)C1=CC(NC(N)=O)=C(O)C=C1

InChI

InChIKey=QHWYYBXPBFQGNI-UHFFFAOYSA-N
InChI=1S/C13H21N3O3.ClH/c1-13(2,3)15-7-11(18)8-4-5-10(17)9(6-8)16-12(14)19;/h4-6,11,15,17-18H,7H2,1-3H3,(H3,14,16,19);1H

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C13H21N3O3
Molecular Weight 267.3241
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 15:25:22 UTC 2023
Edited
by admin
on Fri Dec 15 15:25:22 UTC 2023
Record UNII
G8F3U654FU
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CARBUTEROL HYDROCHLORIDE
MART.   MI   USAN   WHO-DD  
USAN  
Official Name English
Carbuterol hydrochloride [WHO-DD]
Common Name English
CARBUTEROL HYDROCHLORIDE [USAN]
Common Name English
[5-[2-(tert-Butylamino)-1-hydroxyethyl]-2-hydroxyphenyl]urea monohydrochloride
Systematic Name English
CARBUTEROL HYDROCHLORIDE [MI]
Common Name English
SK&F 40383
Code English
CARBUTEROL HCL
Common Name English
UREA, (5-(2-((1,1-DIMETHYLETHYL)AMINO)-1-HYDROXYETHYL)-2-HYDROXYPHENYL)-, MONOHYDROCHLORIDE
Common Name English
SK&F-40383
Code English
CARBUTEROL HYDROCHLORIDE [MART.]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C48149
Created by admin on Fri Dec 15 15:25:22 UTC 2023 , Edited by admin on Fri Dec 15 15:25:22 UTC 2023
Code System Code Type Description
PUBCHEM
36975
Created by admin on Fri Dec 15 15:25:22 UTC 2023 , Edited by admin on Fri Dec 15 15:25:22 UTC 2023
PRIMARY
NCI_THESAURUS
C81650
Created by admin on Fri Dec 15 15:25:22 UTC 2023 , Edited by admin on Fri Dec 15 15:25:22 UTC 2023
PRIMARY
EPA CompTox
DTXSID60956352
Created by admin on Fri Dec 15 15:25:22 UTC 2023 , Edited by admin on Fri Dec 15 15:25:22 UTC 2023
PRIMARY
SMS_ID
100000084872
Created by admin on Fri Dec 15 15:25:22 UTC 2023 , Edited by admin on Fri Dec 15 15:25:22 UTC 2023
PRIMARY
CAS
34866-46-1
Created by admin on Fri Dec 15 15:25:22 UTC 2023 , Edited by admin on Fri Dec 15 15:25:22 UTC 2023
PRIMARY
MERCK INDEX
m3102
Created by admin on Fri Dec 15 15:25:22 UTC 2023 , Edited by admin on Fri Dec 15 15:25:22 UTC 2023
PRIMARY Merck Index
EVMPD
SUB01054MIG
Created by admin on Fri Dec 15 15:25:22 UTC 2023 , Edited by admin on Fri Dec 15 15:25:22 UTC 2023
PRIMARY
ECHA (EC/EINECS)
252-255-4
Created by admin on Fri Dec 15 15:25:22 UTC 2023 , Edited by admin on Fri Dec 15 15:25:22 UTC 2023
PRIMARY
ChEMBL
CHEMBL2110780
Created by admin on Fri Dec 15 15:25:22 UTC 2023 , Edited by admin on Fri Dec 15 15:25:22 UTC 2023
PRIMARY
FDA UNII
G8F3U654FU
Created by admin on Fri Dec 15 15:25:22 UTC 2023 , Edited by admin on Fri Dec 15 15:25:22 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY