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N-phenyl-2-(phenylsulfonyl)hydrazinecarboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

80828-07-5

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80828-07-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80828-07-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,8,2 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 80828-07:
(7*8)+(6*0)+(5*8)+(4*2)+(3*8)+(2*0)+(1*7)=135
135 % 10 = 5
So 80828-07-5 is a valid CAS Registry Number.

80828-07-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(benzenesulfonamido)-3-phenylurea

1.2 Other means of identification

Product number -
Other names N-benzenesulfonyl-N'-phenylsemicarbazide

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:80828-07-5 SDS

80828-07-5Downstream Products

80828-07-5Relevant 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.

STRUCTURE AND REACTIVITY OF HYDRAZINE DERIVATIVES. XLII. KINETICS OF THE REACTIONS OF BENZENESULFONOHYDRAZIDE WITH PHENYL ISOCYANATE IN BENEZENE WITH ADDITIONS OF TRANSITION-METAL ACETYLACETONATES

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

, p. 1131 - 1137 (2007/10/02)

The kinetics were studied for the reactions of benzenesulfonohydrazide with phenyl isocyanate in benzene at various temperatures in the presence of catalytic amounts of transition-metal (Cr3+, Fe3+, Co3+, Co2+,

STRUCTURE AND REACTIVITY OF HYDRAZINE DERIVATIVES. XLI. REACTION OF BENZENESULFONOHYDRAZIDE WITH PHENYL ISOCYANATE IN MIXTURES OF DIOXANE AND WATER

Grekov, A. P.,Veselov, V. Ya.,Kachorovskaya, O. P.

, p. 961 - 965 (2007/10/02)

The kinetics of the reaction of benzenesulfonohydrazide with phenyl isocyanate in mixtures of dioxane and water were investigated.The reaction rate is determined by the effect of nonspecific solvation of the reagents and by the characteristics of the ther

N-(Phenylsulfonyl)- and N-Methyl-N-(phenylsulfonyl)benzohydrazonyl Azides. Thermally Induced Cyclization to Tetrazoles and Decomposition to Benzonitriles

Ito, Suketaka,Tanaka, Yumo,Kakehi, Akikazu

, p. 539 - 543 (2007/10/02)

N-(phenylsulfonyl)- and N-methyl-N-(phenylsulfonyl)benzohydrazonoyl azides, prepared from the corresponding hydrazonoyl chlorides and sodium azide, undergo the cyclization to 5-phenyl-1-(1-phenylsulfonylamino)-1H-tetrazoles together with the competitive decomposition to benzonitriles and the Curtius-type rearrangement leading to semicarbazides when heated in benzene under reflux.The tetrazole formation of hydrazonoyl azides may be characteristic od such hydrazonoyl azides as those carrying an N-sulfonyl substituent, the strong electron-withdrawing nature of which probably promotes the cyclization.

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