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Used in Pharmaceutical Industry:
1H-3-Benzazepine-7,8-diol,2,3,4,5-tetrahydro-1-phenyl-, hydrochloride (1:1), (1R)is used as a pharmaceutical compound for its potential applications in treating neurological and psychiatric conditions. Its specific chemical structure and properties make it a promising candidate for the development of new medications to address these health issues.

81702-42-3

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81702-42-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81702-42-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,7,0 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 81702-42:
(7*8)+(6*1)+(5*7)+(4*0)+(3*2)+(2*4)+(1*2)=113
113 % 10 = 3
So 81702-42-3 is a valid CAS Registry Number.

81702-42-3 Well-known Company Product Price

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  • Sigma

  • (S101)  (R)-(+)-SKF-38393 hydrochloride  ≥98% (HPLC), solid

  • 81702-42-3

  • S101-5MG

  • 2,277.99CNY

  • Detail

  • Sigma

  • (S101)  (R)-(+)-SKF-38393 hydrochloride  ≥98% (HPLC), solid

  • 81702-42-3

  • S101-100MG

  • 20,978.10CNY

  • Detail

81702-42-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (5R)-5-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine-7,8-diol,hydrochloride

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:81702-42-3 SDS

81702-42-3Downstream Products

81702-42-3Relevant academic research and scientific papers

Stereoisomeric probes for the D1 dopamine receptor: synthesis and characterization of R-(+) and S-(-) enantiomers of 3-allyl-7,8-dihydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine and its 6-bromo analogue.

Neumeyer,Kula,Baldessarini,Baindur

, p. 1466 - 1471 (2007/10/02)

Substituted 1-phenyl-3-benzazepines (e.g., SKF 38393 and fenoldopam) exhibit stereoselectivity in moderately high-affinity binding to and partial agonist activation of D1 dopamine receptors. The 3-allyl (APB) and the 3-allyl-6-chloro (6-Cl-APB) analogues

Absolute stereochemistry and dopaminergic activity of enantiomers of 2,3,4,5-tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine

Kaiser,Dandridge,Garvey,Hahn,Sarau,Setler,Bass,Clardy

, p. 697 - 703 (2007/10/02)

Resolution of the unique dopamine receptor agonist 2,3,4,5-tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine (1) was achieved by a stereospecific multistep conversion of the readily separated enantiomers of its O,O,N-trimethylated diffractometric analysi

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