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81633-77-4

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81633-77-4 Usage

Uses

SKF 38393 Hydrobromide is a derivative of a unique dopamine receptor agonist.

Biological Activity

Prototypical D 1 -like dopamine receptor selective partial agonist (K i values are 1, ~ 0.5, ~ 150, ~ 5000 and ~ 1000 nM for D 1 , D 5 , D 2 , D 3 and D 4 receptors respectively).

Check Digit Verification of cas no

The CAS Registry Mumber 81633-77-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,6,3 and 3 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 81633-77:
(7*8)+(6*1)+(5*6)+(4*3)+(3*3)+(2*7)+(1*7)=134
134 % 10 = 4
So 81633-77-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H17NO2.BrH/c18-15-8-12-6-7-17-10-14(13(12)9-16(15)19)11-4-2-1-3-5-11;/h1-5,8-9,14,17-19H,6-7,10H2;1H

81633-77-4SDS

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 (±)-1-Phenyl-2,3,4,5-tetrahydro-(1H)-3-benzazepine-7,8-diolhydrobromide

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:81633-77-4 SDS

81633-77-4Upstream product

81633-77-4Downstream Products

81633-77-4Relevant articles and documents

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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