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Details

Stereochemistry RACEMIC
Molecular Formula C19H23NO6.ClH
Molecular Weight 397.85
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BUTOCROLOL HYDROCHLORIDE

SMILES

Cl.CC1=CC(=O)C2=C(O)C3=C(OC=C3)C(OCC(O)CNC(C)(C)C)=C2O1

InChI

InChIKey=OMNXUSQATUXCBP-UHFFFAOYSA-N
InChI=1S/C19H23NO6.ClH/c1-10-7-13(22)14-15(23)12-5-6-24-16(12)18(17(14)26-10)25-9-11(21)8-20-19(2,3)4;/h5-7,11,20-21,23H,8-9H2,1-4H3;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 C19H23NO6
Molecular Weight 361.389
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Butocrolol amino alcohol derivative with β-adrenolytic, antiarrhythmic, and local anesthetic properties having sympatholytic and antiarrhythmic effects comparable to those of propranolol, but with lower local anesthetic effects.

Approval Year

Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 10:28:57 GMT 2023
Edited
by admin
on Sat Dec 16 10:28:57 GMT 2023
Record UNII
9S6M5WWT6P
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BUTOCROLOL HYDROCHLORIDE
Common Name English
5H-FURO(3,2-G)(1)BENZOPYRAN-5-ONE, 9-(3-((1,1-DIMETHYLETHYL)AMINO)-2-HYDROXYPROPOXY)-4-HYDROXY-7-METHYL-, HYDROCHLORIDE (1:1)
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID80970510
Created by admin on Sat Dec 16 10:28:57 GMT 2023 , Edited by admin on Sat Dec 16 10:28:57 GMT 2023
PRIMARY
FDA UNII
9S6M5WWT6P
Created by admin on Sat Dec 16 10:28:57 GMT 2023 , Edited by admin on Sat Dec 16 10:28:57 GMT 2023
PRIMARY
PUBCHEM
23621042
Created by admin on Sat Dec 16 10:28:57 GMT 2023 , Edited by admin on Sat Dec 16 10:28:57 GMT 2023
PRIMARY
CAS
55165-36-1
Created by admin on Sat Dec 16 10:28:57 GMT 2023 , Edited by admin on Sat Dec 16 10:28:57 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY