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156154-10-8

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156154-10-8 Usage

Chemical origin

Derived from piperazine, a heterocyclic amine.

Core structure

Consists of a 1,4-benzodioxin core, which is a six-membered ring fused to a five-membered ring containing two oxygen atoms.

Molecular composition

A piperazine derivative with the benzodioxin core.

Pharmaceutical applications

Has potential pharmaceutical applications due to its pharmacological properties.

Serotonin receptor agonist

Studied for its potential as a serotonin receptor agonist, which may have implications for the treatment of various conditions.

Treatment of disorders

Investigated for its potential use in the treatment of neurological and psychiatric disorders.

Research interest

The chemical structure and properties of 1,4-Benzodioxin, piperazine deriv. make it a subject of interest for researchers and pharmaceutical companies.

Drug development

Its unique structure and properties are being explored for the development of new drugs targeting specific receptors and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 156154-10-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,1,5 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 156154-10:
(8*1)+(7*5)+(6*6)+(5*1)+(4*5)+(3*4)+(2*1)+(1*0)=118
118 % 10 = 8
So 156154-10-8 is a valid CAS Registry Number.

156154-10-8Downstream Products

156154-10-8Relevant articles and documents

Process for the Preparation of Doxazosin and Salts Thereof

-

, (2012/03/08)

The present invention relates to a process for the preparation of doxazosin or salts thereof.

Conversion of modification D to modification A of doxazosin mesylate

-

, (2008/06/13)

A process for preparing doxazosin mesylate in modification A which comprises dissolving doxazosin with methanesulfonic acid in methanol or a mixture of an aprotic, polar organic solvent and methanol, removing any turbidity from the resulting solution, and

Practical chemical and enzymatic technologies for (S)-1,4-benzodioxan-2-carboxypiperizine intermediate in the synthesis of (S)-doxazosin mesylate

Fang,Grover, Paul,Han, Zhengxu,McConville, Fran X.,Rossi, Richard F.,Olsson, Damase J.,Kessler, Donald W.,Wald, Stephen A.,Senanayake, Chris H.

, p. 2169 - 2174 (2007/10/03)

(S)-1,4-Benzodioxan-2-carboxypiperazine (S)-2, the key chiral intermediate for the synthesis of (S)-doxazosin, was prepared utilizing two approaches: (i) enzymatic resolution of ethyl 1,4-benzodioxan-2-carboxylate with an esterase (Serratia) followed by amide formation; (ii) direct resolution of 1,4-benzodioxan-2-carboxypiperazine 2 with D-tartaric acid. An efficient process for the conversion of (S)-2 to (S)-doxazosin mesylate was developed (80% yield, 99.9% e.e.).

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