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35762-73-3

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35762-73-3 Usage

General Description

4,6-DIMETHYL-PYRIMIDINE-2-SULFONYL FLUORIDE is a chemical compound that belongs to the class of pyrimidines. It contains a sulfonyl fluoride group and is substituted with two methyl groups at the 4 and 6 positions on the pyrimidine ring. 4,6-DIMETHYL-PYRIMIDINE-2-SULFONYL FLUORIDE has the potential for use as a building block in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It is also used as a reagent in chemical reactions, particularly in the formation of carbon-fluorine bonds. Additionally, 4,6-DIMETHYL-PYRIMIDINE-2-SULFONYL FLUORIDE has shown potential as an intermediate in the synthesis of valuable compounds for various industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 35762-73-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,7,6 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 35762-73:
(7*3)+(6*5)+(5*7)+(4*6)+(3*2)+(2*7)+(1*3)=133
133 % 10 = 3
So 35762-73-3 is a valid CAS Registry Number.

35762-73-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6-dimethylpyrimidine-2-sulfonyl fluoride

1.2 Other means of identification

Product number -
Other names 4,6-Dimethyl-pyrimidin-2-sulfonylfluorid

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:35762-73-3 SDS

35762-73-3Downstream Products

35762-73-3Relevant articles and documents

Sulfonyl Fluoride Synthesis through Electrochemical Oxidative Coupling of Thiols and Potassium Fluoride

Laudadio, Gabriele,Bartolomeu, Aloisio De A.,Verwijlen, Lucas M. H. M.,Cao, Yiran,De Oliveira, Kleber T.,No?l, Timothy

supporting information, p. 11832 - 11836 (2019/08/26)

Sulfonyl fluorides are valuable synthetic motifs for a variety of applications, among which sulfur(VI) fluoride exchange-based "click chemistry" is currently the most prominent. Consequently, the development of novel and efficient synthetic methods to access these functional groups is of great interest. Herein, we report a mild and environmentally benign electrochemical approach to prepare sulfonyl fluorides using thiols or disulfides, as widely available starting materials, in combination with KF, as an inexpensive, abundant and safe fluoride source. No additional oxidants nor additional catalysts are required and, due to mild reaction conditions, the reaction displays a broad substrate scope, including a variety of alkyl, benzyl, aryl and heteroaryl thiols or disulfides.

Simple pyrimidines. XIV. The formation and reactions of some derivatives of simple pyrimidinesulphonic acids.

Brown,Hoskins

, p. 522 - 527 (2007/10/04)

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