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3-allyl-6-chloro-7,8-dimethoxy-1-(4-methoxyphenyl)2,3,4,5-tetrahydro-1H-3-benzazepine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77386-10-8

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77386-10-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77386-10-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,3,8 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 77386-10:
(7*7)+(6*7)+(5*3)+(4*8)+(3*6)+(2*1)+(1*0)=158
158 % 10 = 8
So 77386-10-8 is a valid CAS Registry Number.

77386-10-8Downstream Products

77386-10-8Relevant academic research and scientific papers

Dopamine receptor agonists: 3-Allyl-6-chloro-2,3,4,5-tetrahydro-1-(4-hydroxyphenyl)-1H-3-benzazepine-7 ,8-diol and a series of related 3-benzazepines

Ross,Franz,Wilson,Brenner,DeMarinis,Hieble,Sarau

, p. 733 - 740 (2007/10/02)

The N-allyl derivative (SK&F 85174) of 6-chloro-2,3,4,5-tetrahydro-1-(4-hydroxyphenyl)-1H-3-benzazepine-7,8-diol (SK&F 82526) not only retains the exceptional D-1 agonist potency of its parent but also displays reasonably potent D-2 agonist activity, as m

3-Allyl-7,8-dihydroxy-6-halo-1-(4-hydroxyphenyl)-2,3,4,5-tetrahydro-1H-3-benzazepine derivatives

-

, (2008/06/13)

3-Allyl-7,8-dihydroxy-6-halo-1-(4-hydroxyphenyl)-2,3,4,5-tetrahydro-1H-3-benzazepine derivatives are prepared by N-allylation of 7,8-dimethoxy-6-halo-1-(4-methoxyphenyl)-2,3,4,5-tetrahydro-1H-3-benzazepine using an allyl halide in acetonitrile in the presence of base followed by O-demethylation. These compounds have a unique cardiovascular effect in that they are potent renal vasodilators and also induce bradycardia.

7,8-Dihydroxy-1-(sulfamylphenyl)-2,3,4,5-tetrahydro-1H-3-benzazepine derivatives

-

, (2008/06/13)

New 7,8-dihydroxy-1-(sulfamylphenyl)-2,3,4,5-tetrahydro-1H-3-benzazepines having pharmaceutical activity together with new intermediates and methods of synthesis for preparing them. The lead compound is 6-chloro-7,8-dihydroxy-1-(p-sulfamylphenyl)-2,3,4,5-

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