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N-(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)-4-methylbenzenesulfonamide is a complex organic compound with the molecular formula C11H11N3O4S. It is a derivative of pyrimidine, a heterocyclic aromatic organic compound, and is characterized by the presence of a 4-methylbenzenesulfonamide group attached to the pyrimidine ring. This chemical is known for its potential applications in pharmaceuticals and as a chemical intermediate in the synthesis of various compounds. Its structure features a tetrahydropyrimidine ring with two oxygen atoms at the 2 and 4 positions, forming a dioxo group, and a 4-methylbenzenesulfonamide group that contributes to its reactivity and potential therapeutic properties.

6336-23-8

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6336-23-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6336-23-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6336-23:
(6*6)+(5*3)+(4*3)+(3*6)+(2*2)+(1*3)=88
88 % 10 = 8
So 6336-23-8 is a valid CAS Registry Number.

6336-23-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2,4-dioxo-1H-pyrimidin-5-yl)-4-methylbenzenesulfonamide

1.2 Other means of identification

Product number -
Other names benzenesulfonamide,4-methyl-n-(1,2,3,4-tetrahydro-2,4-dioxo-5-pyrimidinyl)

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:6336-23-8 SDS

6336-23-8Downstream Products

6336-23-8Relevant academic research and scientific papers

An Efficient Synthesis and in vitro Cytostatic Activity of 5-Aminosulfonyl Uracil Derivatives

Ismaili, Hamit,Ban, ?eljka,Mati?, Josipa,Safti?, Dijana,Juki?, Marijana,Glava?-Obrovac, Ljubica,?ini?, Biserka

, p. 269 - 277 (2019/12/14)

Efficient synthesis of 5-aminosulfonyl uracil derivatives 2?9 and results of their antiproliferative activity are provided. Sulfonylation of the amino group in 5-aminouracil 1 with selected arylsulfonyl chlorides occurs regioselectively when the reaction

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