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118654-15-2

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118654-15-2 Usage

Parent compound

Piperazine, a heterocyclic compound with two nitrogen atoms in the ring structure.

Form

Dihydrochloride salt, enhancing water solubility.

Solubility

Easily soluble in water, making it convenient for laboratory and industrial processes.

Psychopharmacological potential

Studied for its potential applications in the treatment of psychiatric disorders.

Use as a reagent

Utilized in organic synthesis, particularly in the preparation of various heterocyclic compounds.

Versatility

Possesses a range of potential industrial and pharmaceutical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 118654-15-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,6,5 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 118654-15:
(8*1)+(7*1)+(6*8)+(5*6)+(4*5)+(3*4)+(2*1)+(1*5)=132
132 % 10 = 2
So 118654-15-2 is a valid CAS Registry Number.

118654-15-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-3-phenylpiperazine,dihydrochloride

1.2 Other means of identification

Product number -
Other names 1-METHYL-3-PHENYLPIPERAZINE 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:118654-15-2 SDS

118654-15-2Upstream product

118654-15-2Downstream Products

118654-15-2Relevant articles and documents

Practical and scalable synthesis of orthogonally protected-2-substituted chiral piperazines

Chamakuri, Srinivas,Santini, Conrad,Shah, Manuj M.,Yang, David C. H.,Young, Damian W.

, p. 8844 - 8849 (2020/11/23)

A synthetic route to orthogonally protected, enantiomerically pure 2-substituted piperazines is described. Starting from α-amino acids, within four steps chiral 2-substituted piperazines are obtained. The key transformation involves an aza-Michael additio

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