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Details

Stereochemistry RACEMIC
Molecular Formula C19H23NO2.ClH
Molecular Weight 333.852
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ELUCAINE HYDROCHLORIDE

SMILES

Cl.CCN(CC)CC(OC(=O)C1=CC=CC=C1)C2=CC=CC=C2

InChI

InChIKey=GGAYVDXVPOEEAO-UHFFFAOYSA-N
InChI=1S/C19H23NO2.ClH/c1-3-20(4-2)15-18(16-11-7-5-8-12-16)22-19(21)17-13-9-6-10-14-17;/h5-14,18H,3-4,15H2,1-2H3;1H

HIDE SMILES / InChI
Molecular Formula C19H23NO2
Molecular Weight 297.3914
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )
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

Description

Elucaine is local anesthetic and anti-ulcerative agent, acting as a gastric muscarinic acetylcholine receptor antagonist.

Approval Year

Unknown
149124
Substance Class Chemical
Created
by admin
on Mon Mar 31 23:35:35 GMT 2025
Edited
by admin
on Mon Mar 31 23:35:35 GMT 2025
Record UNII
0IPF408Y2Y
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BENZENEMETHANOL, .ALPHA.-((DIETHYLAMINO)METHYL)-, 1-BENZOATE, HYDROCHLORIDE
Preferred Name English
ELUCAINE HYDROCHLORIDE
Common Name English
Code System Code Type Description
PUBCHEM
32330
Created by admin on Mon Mar 31 23:35:35 GMT 2025 , Edited by admin on Mon Mar 31 23:35:35 GMT 2025
PRIMARY
CAS
24357-99-1
Created by admin on Mon Mar 31 23:35:35 GMT 2025 , Edited by admin on Mon Mar 31 23:35:35 GMT 2025
PRIMARY
EPA CompTox
DTXSID30947212
Created by admin on Mon Mar 31 23:35:35 GMT 2025 , Edited by admin on Mon Mar 31 23:35:35 GMT 2025
PRIMARY
FDA UNII
0IPF408Y2Y
Created by admin on Mon Mar 31 23:35:35 GMT 2025 , Edited by admin on Mon Mar 31 23:35:35 GMT 2025
PRIMARY
Related Record Type Details
Structure of ELUCAINE HYDROCHLORIDE, (S)-
ENANTIOMER -> RACEMATE
Structure of ELUCAINE HYDROCHLORIDE, (R)-
ENANTIOMER -> RACEMATE
Related Record Type Details
Structure of ELUCAINE
ACTIVE MOIETY
NIH
NCATS
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