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Benzoic acid, 2-(iminophenylmethyl)hydrazide, also known as 2-(benzylamino)benzoic acid hydrazide, is a chemical compound with the molecular formula C14H14N2O2. It is a white crystalline solid that is soluble in water and various organic solvents. Benzoic acid, 2-(iminophenylmethyl)hydrazide is formed by the condensation of benzoic acid with 2-(iminophenylmethyl)hydrazine, resulting in the formation of a hydrazide group. It is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of herbicides and other chemical compounds. Due to its reactivity and potential applications, it is an important compound in the field of organic chemistry and chemical engineering.

4057-68-5

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4057-68-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4057-68-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,5 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4057-68:
(6*4)+(5*0)+(4*5)+(3*7)+(2*6)+(1*8)=85
85 % 10 = 5
So 4057-68-5 is a valid CAS Registry Number.

4057-68-5SDS

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 N-benzoyl-benzamidrazone

1.2 Other means of identification

Product number -
Other names N-(α-Imino-benzyl)-N'-benzoyl-hydrazin

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:4057-68-5 SDS

4057-68-5Relevant academic research and scientific papers

C-(β-d-Glucopyranosyl)formamidrazones, formic acid hydrazides and their transformations into 3-(β-d-glucopyranosyl)-5-substituted-1,2,4- triazoles: A synthetic and computational study

Bokor, éva,Fekete, Attila,Varga, Gergely,Szocs, Béla,Czifrák, Katalin,Komáromi, István,Somsák, László

, p. 10391 - 10404 (2013/11/19)

Synthesis of O-perbenzoylated 3-(β-d-glucopyranosyl)-5-substituted-1, 2,4-triazoles, precursors of potent inhibitors of glycogen phosphorylase, was studied by ring closures of N1-acyl-carboxamidrazone type intermediates. Reactions of C-(β-d-glu

A New Class of Nonhormonal Pregnancy-Terminating Agents. Synthesis and Contragestational Activity of 3,5-Diaryl-s-triazoles

Omodei-Sale, Amedeo,Consonni, Pietro,Galliani, Giulio

, p. 1187 - 1192 (2007/10/02)

A series of 3,5-diaryl-s-triazoles were synthesized and evaluated as postimplantation contragestational agents.The introduction of various substituents (e.g., an o-alkyl chain on one phenyl and a m-alkoxy group on the other) was found to increase the potency.Several compounds with very high pregnancy-terminating activity in both hamsters and rats were obtained.One of these, 3-(2-ethylphenyl)-5-(3-methoxyphenyl)-s-triazole, DL 111 (36), was selected for detailed evaluation in various animal species.A synthetic scheme for the preparation of these compounds and preliminary structure-activity relationships are presented.

Metallhydrazide, XIX. Addition bis(diethylaluminio)substituierter Amidrazone und Carbohydrazide an Nitrile

Kauffmann, Thomas,Ban, Laszlo,Kuhlmann, Dieter

, p. 3684 - 3690 (2007/10/02)

Amidrazones and carbohydrazides react with two equivalents of triethylaluminium to give bis(diethylaluminio) derivatives 1 and 7, respectively.In contrast to the corresponding mono(diethylaluminio) derivatives or disodium salts, these are capable of addit

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