Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C9H13NO2 |
Molecular Weight | 167.205 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@H](N)[C@H](O)C1=CC=C(O)C=C1
InChI
InChIKey=JAYBQRKXEFDRER-RCOVLWMOSA-N
InChI=1S/C9H13NO2/c1-6(10)9(12)7-2-4-8(11)5-3-7/h2-6,9,11-12H,10H2,1H3/t6-,9-/m0/s1
Approval Year
PubMed
Title | Date | PubMed |
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Simultaneous determination of amphetamine and one of its metabolites by HPLC with electrochemical detection. | 2002 Sep 5 |
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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 Jan 2 |
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Synthesis and evaluation of uterine relaxant activity for a novel series of substituted p-hydroxyphenylethanolamines. | 2006 Oct 1 |
Patents
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Code System | Code | Type | Description | ||
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p-Hydroxynorephedrine
Created by
admin on Fri Dec 15 15:21:28 GMT 2023 , Edited by admin on Fri Dec 15 15:21:28 GMT 2023
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O6914L7189
Created by
admin on Fri Dec 15 15:21:28 GMT 2023 , Edited by admin on Fri Dec 15 15:21:28 GMT 2023
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DTXSID70902582
Created by
admin on Fri Dec 15 15:21:28 GMT 2023 , Edited by admin on Fri Dec 15 15:21:28 GMT 2023
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771-91-5
Created by
admin on Fri Dec 15 15:21:28 GMT 2023 , Edited by admin on Fri Dec 15 15:21:28 GMT 2023
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6931143
Created by
admin on Fri Dec 15 15:21:28 GMT 2023 , Edited by admin on Fri Dec 15 15:21:28 GMT 2023
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552-85-2
Created by
admin on Fri Dec 15 15:21:28 GMT 2023 , Edited by admin on Fri Dec 15 15:21:28 GMT 2023
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NON-SPECIFIC STEREOCHEMISTRY |
PARENT (METABOLITE)
PARENT (METABOLITE)
SUBSTANCE RECORD