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1-(diphenylmethyl)-4-(prop-2-en-1-yl)piperazine dihydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41332-10-9

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41332-10-9 Usage

Usage

Psychoactive drug (recreational or party drug)

Effects

Hallucinogenic and stimulant effects on the central nervous system

Side effects

Increased heart rate, high blood pressure

Health risks

Potential for addiction

Legal status

Controlled substance in many countries

Legal restrictions

Illegal to possess, manufacture, or distribute without proper authorization

Check Digit Verification of cas no

The CAS Registry Mumber 41332-10-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,3,3 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 41332-10:
(7*4)+(6*1)+(5*3)+(4*3)+(3*2)+(2*1)+(1*0)=69
69 % 10 = 9
So 41332-10-9 is a valid CAS Registry Number.

41332-10-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzhydryl-4-prop-2-enylpiperazine,dihydrochloride

1.2 Other means of identification

Product number -
Other names 1-(Diphenylmethyl)-4-(2-propenyl)piperazine dihydrochloride

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:41332-10-9 SDS

41332-10-9Downstream Products

41332-10-9Relevant academic research and scientific papers

NOVEL WATER BASED PROCESS FOR THE PREPARATION OF SUBSTITUTED DIPHENYLMETHYL PIPERAZINES

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Page/Page column 9, (2011/08/03)

The present invention relates to a novel water based process for the preparation of substituted diphenylmethyl piperazines of Formula I and pharmaceutically acceptable salts wherein X1 and X2 represent independently a hydrogen, a halogen, a straight or branched chain lower alkyl, alkoxy or a hydroxyl radical and R is selected from groups such as acyl, alkyl, alkenyl, aralalkyl, aralalkenyl aralkyl, and aralalkenyl or aralkenyl hydroxyalkyl, aryloxyalkyl, alkoxyalkyl, aminoalkyl or its derivative comprising, reacting a compound of Formula II, with a compound of formula R—X where R is as defined above and X is suitable leaving group which includes halides, but not limiting use of other leaving groups such as tosylate, mesylate and activated acid groups such as acyl halide, anhydrides, mixed anhydrides etc. using water as a solvent, in presence of a catalyst and a base, at 25-100° C.;

N-(3,3-diphenylpropyl)-n'-aralkyl-substituted piperazines

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, (2008/06/13)

N-(3,3-Diphenylpropyl)-N'-aralkyl-substituted piperazines which have a structure in which a hydrogen in the N'-benzene ring has been substituted for by --(OCH3)n (in which n represents an integer from 0 - 3) were synthesized. These compounds are novel compounds that are not found in literature, and have a coronary blood flow increasing action in considerably lower amounts than do conventional piperazine compounds having similar effects.

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