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Benzamide, N-methyl-N-(phenylsulfonyl)-, also known as N-Methyl-N-phenylsulfonylbenzamide, is an organic compound with the chemical formula C14H13NO3S. It is a derivative of benzamide, featuring a methyl group attached to the nitrogen atom and a phenylsulfonyl group (a phenyl group connected to a sulfonyl group) attached to the other nitrogen atom. Benzamide, N-methyl-N-(phenylsulfonyl)- is a white crystalline solid and is used as an intermediate in the synthesis of various pharmaceuticals and chemical compounds. It is characterized by its melting point of 95-97°C and is soluble in common organic solvents such as ethanol and acetone. Due to its reactivity and potential applications, it is important to handle Benzamide, N-methyl-N-(phenylsulfonyl)- with care, following proper safety protocols.

3409-96-9

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3409-96-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3409-96-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,0 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3409-96:
(6*3)+(5*4)+(4*0)+(3*9)+(2*9)+(1*6)=89
89 % 10 = 9
So 3409-96-9 is a valid CAS Registry Number.

3409-96-9SDS

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 N-Methyl-N-(phenylsulfonyl)benzamide

1.2 Other means of identification

Product number -
Other names N-Methyl-N-benzoyl-benzolsulfamid

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:3409-96-9 SDS

3409-96-9Relevant academic research and scientific papers

N-Aroylsulfonamide-Photofragmentation (ASAP)-A Versatile Route to Biaryls

Wessig, Pablo,Krebs, Saskia

supporting information, p. 6367 - 6374 (2021/09/29)

The photochemical fragmentation of N-aroylsulfonamides 9 (ASAP) is a powerful method for the preparation of various biaryls. Compounds 9 are easily accessible in two steps from amines by treatment with arenesulfonyl chlorides and aroyl chlorides. Many of these compounds were prepared for the first time. The irradiation takes place in a previously developed continuous-flow reactor using inexpensive UVB or UVC fluorescent lamps. Isocyanates and sulphur dioxide are formed as the only by-products. The ASAP tolerates a variety of functional groups and is even suited for the preparation of phenylnaphthalenes and terphenyls. The ASAP mechanism was elucidated by interaction of photophysical and quantum chemical (DFT) methods and revealed a spirocyclic biradical as key intermediate.

Development of an acyl sulfonamide anti-proliferative agent, ly573636 ? na

Yates, Matthew H.,Kallman, Neil J.,Ley, Christopher P.,Wei, Jeffrey N.

experimental part, p. 255 - 262 (2010/04/22)

The synthesis of 5-bromo-thiophene-2-sulfonic acid 2,4-dichlo- robenzoylamide sodium salt on multikilogram scale is described. The initial clinical supplies were made using carbonyl diimidazole to converge the two fragments. A more efficient acid chloride process has been developed, which also provides better control of impurities and color throughout the synthesis.

β-Keto sulfones as inhibitors of 11β-hydroxysteroid dehydrogenase type I and the mechanism of action

Xiang, Jason,Ipek, Manus,Suri, Vipin,Tam, May,Xing, Yuzhe,Huang, Nelson,Zhang, Yanling,Tobin, James,Mansour, Tarek S.,McKew, John

, p. 4396 - 4405 (2008/03/12)

The design, synthesis, and biological evaluation of β-keto sulfones as 11β-HSD1 inhibitors and the mechanism of inhibition are described here. This class of compounds is not active against 11β-HSD2 and therefore may have therapeutic potential for metabolic syndrome and type 2 diabetes.

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