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163596-56-3

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163596-56-3 Usage

Description

CINNAMYL PIEPRAZINE HYDROCHLORIDE, also known as trans-1-Cinnamylpiperazine Dihydrochloride, is a chemical compound that serves as a salt of trans-1-Cinnamylpiperazine (C442150). It is characterized by its unique chemical structure and properties, which make it a valuable component in the development of pharmaceuticals and other applications.

Uses

Used in Pharmaceutical Industry:
CINNAMYL PIEPRAZINE HYDROCHLORIDE is used as a key component in the synthesis of bile acid piperazinyl derivatives. These derivatives exhibit pro-apoptotic properties, which means they can induce programmed cell death in carcinoma human cell lines. This makes them a promising avenue for the development of new cancer treatments and therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 163596-56-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,5,9 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 163596-56:
(8*1)+(7*6)+(6*3)+(5*5)+(4*9)+(3*6)+(2*5)+(1*6)=163
163 % 10 = 3
So 163596-56-3 is a valid CAS Registry Number.

163596-56-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-phenylprop-2-enyl)piperazine,hydrochloride

1.2 Other means of identification

Product number -
Other names 1-(3-phenylprop-2-enyl)piperazine hydrochloride

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:163596-56-3 SDS

163596-56-3Downstream Products

163596-56-3Relevant articles and documents

Synthesis method of cinnamyl piperazine

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Paragraph 0016; ; 0017; 0018; 0019, (2017/08/27)

The invention discloses a synthesis method of cinnamyl piperazine. The method includes the steps of: a) adding a solvent into a reaction kettle and adding piperazine to uniformly dissolve the piperazine, dropwisely adding hydrochloric acid at 20-25 DEG C until the pH of the reaction solution is 2, which is the terminal, and after the reaction is performed for 1 h, cooling the reaction solution to 20 DEG C, and centrifugally spin-filtering the reaction solution to obtain piperazine dihydrochloride; b) adding the solvent into the reaction kettle, adding the piperazine dihydrochloride and the piperazine with stirring at the same time, and performing a reaction at 68-85 DEG C for 0.5-3 h; c) reducing the temperature to 45-55 DEG C, dropwisely adding cinnamyl chloride, and then increasing the temperature to 60-75 DEG C to perform a temperature maintained reaction for 1-4 h, and reducing the temperature to 10-35 DEG C, performing centrifugal separation, sucking a mother liquid into a distillation reaction kettle, heating the distillation mother liquid to recycle the solvent, adding pure water, and dropwisely adding an alkali liquid to regulate the pH to 9-12, and adding chloroform to perform extraction, drying the mixture, and evaporate-drying the chloroform to obtain the cinnamyl piperazine. The synthesis method reduces production steps and pollutant emission, and is more suitable for modern industrial production.

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