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
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
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| 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
| Name | Type | Language | ||
|---|---|---|---|---|
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Common Name | English | ||
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Preferred Name | English | ||
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Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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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
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PRIMARY | |||
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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
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PRIMARY | |||
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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
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PRIMARY |
SUBSTANCE RECORD