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Ethanamine, N,N-dimethyl-2-(phenylsulfonyl)-, also known as N,N-dimethyl-2-phenylsulfonylethanamine, is an organic compound with the chemical formula C10H15NO2S. It is a derivative of ethanamine, featuring a phenylsulfonyl group attached to the nitrogen atom. This colorless liquid is soluble in organic solvents and has a molecular weight of 213.29 g/mol. It is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity, it is essential to handle Ethanamine, N,N-dimethyl-2-(phenylsulfonyl)- with care, following proper safety protocols.

3405-93-4

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3405-93-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3405-93-4 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 5 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3405-93:
(6*3)+(5*4)+(4*0)+(3*5)+(2*9)+(1*3)=74
74 % 10 = 4
So 3405-93-4 is a valid CAS Registry Number.

3405-93-4Relevant academic research and scientific papers

SMALL MOLECULE CMKLR1 ANTAGONISTS IN INFLAMMATORY DISEASE

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Paragraph 0287, (2020/12/01)

α-NETA analogs are provided for the treatment of inflammatory disease.

Intramolecular Diels-Alder Reactions of Internally-substituted Trienylsulfones. Synthesis of Bicyclo and - Systems Possessing a Bridgehead Sulfonyl Group

Clasby, Martin C.,Craig, Donald,Slawin, Alexandra M. Z.,White, Andrew J. P.,Williams, David J.

, p. 1509 - 1532 (2007/10/02)

A series of trienes possessing internally-activated vinylic sulfone dienophilic groups undergo intramolecular Diels-Alder (IMDA) reaction with high or complete selectivity for the cis-fused products.Incorporation of silyloxy groups within the carbon tethe

Simple Generation of Nonstabilized Azomethine Ylides through Decarboxylative Condensation of α-Amino Acids with Carbonyl Compounds via 5-Oxazolidinone Intermediates

Tsuge, Otohiko,Kanemasa, Shuji,Ohe, Masayuki,Takenaka, Shigeori

, p. 4079 - 4090 (2007/10/02)

Heating α-amino acids with a variety of carbonyl compounds generates N-unsubstituted or N-substituted azomethine ylides of nonstabilized types through the elimination of water and carbon dioxide.The ylides are captured by olefinic, acetylenic, and carbonyl dipolarophiles producing pyrrolidines, pyrrolines, and oxazolidines.The reaction involves intermediary 5-oxazolidinones which can be sometimes isolated.Some synthetic equivalents of parent azomethine ylide, methaniminium methylide, are accessible by this route.

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