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Details

Stereochemistry RACEMIC
Molecular Formula C10H15NO3.ClH
Molecular Weight 233.692
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N-METHYLEPINEPHRINE HYDROCHLORIDE

SMILES

Cl.CN(C)CC(O)C1=CC=C(O)C(O)=C1

InChI

InChIKey=ONSKRXJOMDVYGQ-UHFFFAOYSA-N
InChI=1S/C10H15NO3.ClH/c1-11(2)6-10(14)7-3-4-8(12)9(13)5-7;/h3-5,10,12-14H,6H2,1-2H3;1H

HIDE SMILES / InChI

Molecular Formula C10H15NO3
Molecular Weight 197.231
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

Approval Year

PubMed

PubMed

TitleDatePubMed
A predominantly adrenaline-secreting phaeochromocytoma.
1990-07
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:53:03 GMT 2025
Edited
by admin
on Mon Mar 31 17:53:03 GMT 2025
Record UNII
8D1B6XEV7G
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
(±)-N-METHYLEPINEPHRINE HYDROCHLORIDE
Preferred Name English
N-METHYLEPINEPHRINE HYDROCHLORIDE
Common Name English
1,2-BENZENEDIOL, 4-(2-(DIMETHYLAMINO)-1-HYDROXYETHYL)-, HYDROCHLORIDE (1:1)
Systematic Name English
DL-N-METHYLEPINEPHRINE HYDROCHLORIDE
Common Name English
Code System Code Type Description
FDA UNII
8D1B6XEV7G
Created by admin on Mon Mar 31 17:53:03 GMT 2025 , Edited by admin on Mon Mar 31 17:53:03 GMT 2025
PRIMARY
CAS
62-22-6
Created by admin on Mon Mar 31 17:53:03 GMT 2025 , Edited by admin on Mon Mar 31 17:53:03 GMT 2025
PRIMARY
EPA CompTox
DTXSID501018938
Created by admin on Mon Mar 31 17:53:03 GMT 2025 , Edited by admin on Mon Mar 31 17:53:03 GMT 2025
PRIMARY
CAS
13076-09-0
Created by admin on Mon Mar 31 17:53:03 GMT 2025 , Edited by admin on Mon Mar 31 17:53:03 GMT 2025
SUPERSEDED
PUBCHEM
71737788
Created by admin on Mon Mar 31 17:53:03 GMT 2025 , Edited by admin on Mon Mar 31 17:53:03 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY