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Details

Stereochemistry RACEMIC
Molecular Formula C20H23NO2.ClH
Molecular Weight 345.863
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AMOLANONE HYDROCHLORIDE

SMILES

Cl.CCN(CC)CCC1(C(=O)OC2=CC=CC=C12)C3=CC=CC=C3

InChI

InChIKey=JLTVLLBWSZPXFN-UHFFFAOYSA-N
InChI=1S/C20H23NO2.ClH/c1-3-21(4-2)15-14-20(16-10-6-5-7-11-16)17-12-8-9-13-18(17)23-19(20)22;/h5-13H,3-4,14-15H2,1-2H3;1H

HIDE SMILES / InChI

Molecular Formula C20H23NO2
Molecular Weight 309.4021
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

PubMed

PubMed

TitleDatePubMed
Studies in urethral anesthesia: tronothane and amethone.
1957
Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:32:05 GMT 2023
Edited
by admin
on Fri Dec 15 15:32:05 GMT 2023
Record UNII
M36927R46E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AMOLANONE HYDROCHLORIDE
MI  
Common Name English
AMOLANONE HCL
Common Name English
3-(2-(DIETHYLAMINO)ETHYL)-3-PHENYL-2(3H)-BENZOFURANONE HYDROCHLORIDE
Systematic Name English
2(3H)-BENZOFURANONE, 3-(2-(DIETHYLAMINO)ETHYL)-3-PHENYL-, HYDROCHLORIDE (1:1)
Systematic Name English
AMOLANONE HYDROCHLORIDE [MI]
Common Name English
2(3H)-BENZOFURANONE, 3-(2-(DIETHYLAMINO)ETHYL)-3-PHENYL-, HYDROCHLORIDE
Systematic Name English
AMETHONE HYDROCHLORIDE
Brand Name English
Classification Tree Code System Code
NCI_THESAURUS C245
Created by admin on Fri Dec 15 15:32:06 GMT 2023 , Edited by admin on Fri Dec 15 15:32:06 GMT 2023
Code System Code Type Description
NCI_THESAURUS
C75084
Created by admin on Fri Dec 15 15:32:06 GMT 2023 , Edited by admin on Fri Dec 15 15:32:06 GMT 2023
PRIMARY
CAS
6009-67-2
Created by admin on Fri Dec 15 15:32:06 GMT 2023 , Edited by admin on Fri Dec 15 15:32:06 GMT 2023
PRIMARY
FDA UNII
M36927R46E
Created by admin on Fri Dec 15 15:32:06 GMT 2023 , Edited by admin on Fri Dec 15 15:32:06 GMT 2023
PRIMARY
MERCK INDEX
m45
Created by admin on Fri Dec 15 15:32:06 GMT 2023 , Edited by admin on Fri Dec 15 15:32:06 GMT 2023
PRIMARY Merck Index
PUBCHEM
22336
Created by admin on Fri Dec 15 15:32:06 GMT 2023 , Edited by admin on Fri Dec 15 15:32:06 GMT 2023
PRIMARY
EPA CompTox
DTXSID30975515
Created by admin on Fri Dec 15 15:32:06 GMT 2023 , Edited by admin on Fri Dec 15 15:32:06 GMT 2023
PRIMARY
ChEMBL
CHEMBL329901
Created by admin on Fri Dec 15 15:32:06 GMT 2023 , Edited by admin on Fri Dec 15 15:32:06 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY