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599-62-2

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599-62-2 Usage

General Description

4,N-DIMETHYL-N-PHENYL-BENZENESULFONAMIDE is a chemical compound that belongs to the group of sulfonamides. It is an organic compound with the molecular formula C14H15NO2S and a molecular weight of 269.34 g/mol. 4,N-DIMETHYL-N-PHENYL-BENZENESULFONAMIDE contains a benzene ring substituted with a sulfonamide group and two methyl groups. 4,N-DIMETHYL-N-PHENYL-BENZENESULFONAMIDE is commonly used as an intermediate in the synthesis of pharmaceuticals and other organic compounds. It has also been studied for its potential biological activities, including anti-inflammatory and antitumor properties. Additionally, it is used in chemical research and as a precursor in the production of various industrial and agricultural chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 599-62-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 599-62:
(5*5)+(4*9)+(3*9)+(2*6)+(1*2)=102
102 % 10 = 2
So 599-62-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H15NO2S/c1-12-8-10-14(11-9-12)18(16,17)15(2)13-6-4-3-5-7-13/h3-11H,1-2H3

599-62-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N,4-dimethyl-N-phenylbenzenesulfonamide

1.2 Other means of identification

Product number -
Other names Benzenesulfonamide,N,4-dimethyl-N-phenyl

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:599-62-2 SDS

599-62-2Relevant articles and documents

A Mild Heteroatom (O -, N -, and S -) Methylation Protocol Using Trimethyl Phosphate (TMP)-Ca(OH) 2Combination

Tang, Yu,Yu, Biao

, (2022/03/27)

A mild heteroatom methylation protocol using trimethyl phosphate (TMP)-Ca(OH)2combination has been developed, which proceeds in DMF, or water, or under neat conditions, at 80 °C or at room temperature. A series of O-, N-, and S-nucleophiles, including phenols, sulfonamides, N-heterocycles, such as 9H-carbazole, indole derivatives, and 1,8-naphthalimide, and aryl/alkyl thiols, are suitable substrates for this protocol. The high efficiency, operational simplicity, scalability, cost-efficiency, and environmentally friendly nature of this protocol make it an attractive alternative to the conventional base-promoted heteroatom methylation procedures.

Debenzylative Sulfonylation of Tertiary Benzylamines Promoted by Visible Light

Fu, Ying,Wu, Qing-Kui,Du, Zhengyin

supporting information, p. 1896 - 1900 (2021/04/06)

An efficient, general, inexpensive, and environmentally friendly photosynthesis of sulfonamides via visible light promoted debenzylative sulfonylation of tertiary benzylamines is described. Compared to the traditional S?N coupling reactions, which are promoted by oxidative C?N bond cleavage of symmetrical tertiary alkylamines, this strategy provides a selective C?N bond cleavage protocol and avoids the use of transition-metal, explosive oxidants, and ligands.

KMnO4-mediated oxidative C[sbnd]N bond cleavage of tertiary amines: Synthesis of amides and sulfonamides

Zhang, Zhang,Liu, Yong-Hong,Zhang, Xi,Wang, Xi-Cun

, p. 2763 - 2770 (2019/04/10)

KMnO4-mediated oxidative C[sbnd]N bond cleavage of tertiary amines producing secondary amine was introduced, which was trapped by electrophiles (acyl chloride and sulfonyl chloride) to form amides and sulfonamides. The reaction could take place at mild condition, tolerating a wide range of function groups and affording products in moderate to excellent yields.

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