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Hydrazinecarboxamide, 2-[(4-methylphenyl)sulfonyl]-N-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

28744-07-2

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28744-07-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28744-07-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,7,4 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 28744-07:
(7*2)+(6*8)+(5*7)+(4*4)+(3*4)+(2*0)+(1*7)=132
132 % 10 = 2
So 28744-07-2 is a valid CAS Registry Number.

28744-07-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(4-methylphenyl)sulfonylamino]-3-phenylurea

1.2 Other means of identification

Product number -
Other names 1-Tosyl-4-phenylsemicarbazid

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:28744-07-2 SDS

28744-07-2Downstream Products

28744-07-2Relevant academic research and scientific papers

Design, synthesis and SAR of novel sulfonylurea derivatives for the treatment of Diabetes mellitus in rats

Sroor, Farid M.,Basyouni, Wahid M.,Aly, Hanan F.,Ali, Sanaa A.,Arafa, Azza F.

, p. 195 - 206 (2021/12/01)

Novel series of sulfonylurea analogs were designed, synthesized and fully characterized. The targeted sulfonylurea analogs 3–11, were prepared in a straight forward manner by nucleophilic addition of aryl-sulfonyl hydrazine derivatives 1a–c to alkyl- or a

STRUCTURE AND REACTIVITY OF HYDRAZINE DERIVATIVES: XLIV. SPECIFIC AND NONSPECIFIC EFFECT OF SOLVENTS IN THE REACTION OF ARENESULFONOHYDRAZIDES WITH PHENYL ISOCYANATE

Veselov, V. Ya.,Shat-skaya, V. A.,Zhurilo, A. A.,Grekov, A. P.

, p. 949 - 952 (2007/10/02)

The kinetics of the reaction of arenesulfonohydrazides with phenyl isocyanate in various types of solvents were studied.Quantitative treatment of the effects of the structure of the arenesulfonohydrazides and the medium on the rate of the reaction showed

STRUCTURE AND REACTIVITY OF HYDRAZINE DERIVATIVES. XLIII. REACTION OF ISOCYANATES WITH ARENESULFONOHYDRAZIDES IN THE PRESENCE OF SOME TRANSITION-METAL β-DIKETONATES IN DIOXANE

Grekov, A. P.,Savel'ev, Yu. V.,Veselov, V. Ya.

, p. 2324 - 2331 (2007/10/02)

The kinetics of the reactions of 1-butyl isocyanate and phenyl isocyanate with arenesulfonohydrazides in dioxane at various temperatures with additions of zinc(II) and iron(III) acetylacetonates, which exhibit a catalytic effect, were studied.It was established that intermediate "catalyst-isocyanate" and "catalyst-hydrazide" molecular complexes are formed in the reactions.A quantitative estimate of the catalytic activity of the investigated metal β-diketonates is given.

Synthesis of sulfonyl semicarbazides

-

, (2008/06/13)

A new synthetic route to sulfonyl semicarbazides (sulfonyldiazanecarboxamides) and sulfonyl-1,2-diazanedicarboxyamide wherein a substituted 1,2-diazenedicarboxamide is reacted with a salt of a sulfinic acid.

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