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4-Benzyl-1-piperazin-carboxylic acid amide HCl is a piperazine derivative chemical compound used as an intermediate in the pharmaceutical industry for the synthesis of various drugs. It features a benzyl group attached to the piperazine ring and a carboxylic acid amide functional group, with the HCl salt form enhancing its stability and solubility for pharmaceutical applications.

89026-61-9

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89026-61-9 Usage

Uses

Used in Pharmaceutical Industry:
4-Benzyl-1-piperazin-carboxylic acid amide HCl is used as a chemical intermediate for the synthesis of antipsychotic, antihistaminic, and other pharmaceutical agents. Its unique structure allows it to be a key component in the development of new drug candidates.
It is important to handle 4-Benzyl-1-piperazin-carboxylic acid amide HCl with proper safety precautions and in accordance with regulatory guidelines due to its potential health and environmental hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 89026-61-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,0,2 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 89026-61:
(7*8)+(6*9)+(5*0)+(4*2)+(3*6)+(2*6)+(1*1)=149
149 % 10 = 9
So 89026-61-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H17N3O.ClH/c13-12(16)15-8-6-14(7-9-15)10-11-4-2-1-3-5-11;/h1-5H,6-10H2,(H2,13,16);1H

89026-61-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-benzylpiperazine-1-carboxamide

1.2 Other means of identification

Product number -
Other names 4-benzyl-piperazine-1-carboxylic acid amide

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:89026-61-9 SDS

89026-61-9Relevant academic research and scientific papers

N-Acyl-N'-(pyridin-2-yl) Ureas and Analogs Exhibiting Anti-Cancer and Anti-Proliferative Activities

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Paragraph 0381, (2014/09/29)

Described are compounds of Formula 1 which find utility in the treatment of cancer, autoimmune diseases and metabolic bone disorders through inhibition of c-FMS (CSF-1R), c-KIT, and/or PDGFR kinases. These compounds also find utility in the treatment of other mammalian diseases mediated by c-FMS, c-KIT, or PDGFR kinases.

The Dehydration of Ureas by Two-Phase Dichlorocarbene Reaction, a Synthetic Access to Substituted Cyanamides

Schroth, W.,Kluge, H.,Frach, R.,Hodek, W.,Schaedler, H. D.

, p. 787 - 802 (2007/10/02)

A wide variety of N,N-disubstituted ureas are dehydrated in the CHCl3/NaOH catalytic two-phase system under mild conditions.The sequence of urea-transamidation and dehydration thus offers a profitable approach to aprotic cyanamides.Among various tested PT-catalysts tertiary amines prove to be the most efficient and favourable ones.Tertiary amines may also be used advantageously in the transformation of carboxylic amides and thioamides to the corresponding nitriles.The application of the same technique is less suitable in the case of N-mono-substituted ureas, N,N'-disubstituted ureas as well as N(dialkylaminomethylidene)ureas, because consequent reactions of the primarily formed cyanamides predominate.Problems concerning the dehydration mechanism are elucidated in terms of HMO-perturbation theory.

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