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4-phenylpiperazine-1-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77464-11-0

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77464-11-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77464-11-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,4,6 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 77464-11:
(7*7)+(6*7)+(5*4)+(4*6)+(3*4)+(2*1)+(1*1)=150
150 % 10 = 0
So 77464-11-0 is a valid CAS Registry Number.

77464-11-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-phenylpiperazine-1-carboxamide

1.2 Other means of identification

Product number -
Other names 4-phenyl-piperazine-1-carbothioic acid anilide

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:77464-11-0 SDS

77464-11-0Relevant academic research and scientific papers

Synthesis and Antiallergy Activity of N--4-aryl-1-piperazinecarboxamide Derivatives

Walsh, David A.,Green, Jerry B.,Franzyshen, Stephen K.,Nolan, Joseph C.,Yanni, John M.

, p. 2028 - 2032 (2007/10/02)

A series of N--4-aryl-1-piperazinecarboxamides was synthesized and evaluated for antiallergy activity.Several derivatives had activity in the passive foot anaphylaxis (PFA) assay, an IgE-mediated model useful in the detection of co

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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