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Details

Stereochemistry ABSOLUTE
Molecular Formula C9H13NO2.ClH
Molecular Weight 203.666
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of P-HYDROXYNOREPHEDRINE HYDROCHLORIDE

SMILES

Cl.C[C@H](N)[C@H](O)C1=CC=C(O)C=C1

InChI

InChIKey=AYEOOGDUDIHXQE-YDYUUSCQSA-N
InChI=1S/C9H13NO2.ClH/c1-6(10)9(12)7-2-4-8(11)5-3-7;/h2-6,9,11-12H,10H2,1H3;1H/t6-,9-;/m0./s1

HIDE SMILES / InChI

Molecular Formula C9H13NO2
Molecular Weight 167.205
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

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
Synthesis and evaluation of uterine relaxant activity for a novel series of substituted p-hydroxyphenylethanolamines.
2006-10-01
Relationship between stereochemistry and the beta3-adrenoceptor agonistic activity of 4'-hydroxynorephedrine derivative as an agent for treatment of frequent urination and urinary incontinence.
2003-01-02
Simultaneous determination of amphetamine and one of its metabolites by HPLC with electrochemical detection.
2002-09-05
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:00:24 GMT 2025
Edited
by admin
on Mon Mar 31 18:00:24 GMT 2025
Record UNII
49PJ7A9JWQ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
P-HYDROXYNOREPHEDRINE HYDROCHLORIDE
Common Name English
BENZENEMETHANOL, .ALPHA.-((1S)-1-AMINOETHYL)-4-HYDROXY-, HYDROCHLORIDE (1:1), (.ALPHA.R)-
Preferred Name English
BENZENEMETHANOL, .ALPHA.-(1-AMINOETHYL)-4-HYDROXY-, HYDROCHLORIDE, (R-(R*,S*))-
Systematic Name English
Code System Code Type Description
PUBCHEM
10285871
Created by admin on Mon Mar 31 18:00:24 GMT 2025 , Edited by admin on Mon Mar 31 18:00:24 GMT 2025
PRIMARY
CAS
3240-42-4
Created by admin on Mon Mar 31 18:00:24 GMT 2025 , Edited by admin on Mon Mar 31 18:00:24 GMT 2025
PRIMARY
FDA UNII
49PJ7A9JWQ
Created by admin on Mon Mar 31 18:00:24 GMT 2025 , Edited by admin on Mon Mar 31 18:00:24 GMT 2025
PRIMARY