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Isothiazole, 4,5-dihydro-3-phenyl-, 1,1-dioxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

881652-47-7

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881652-47-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 881652-47-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,1,6,5 and 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 881652-47:
(8*8)+(7*8)+(6*1)+(5*6)+(4*5)+(3*2)+(2*4)+(1*7)=197
197 % 10 = 7
So 881652-47-7 is a valid CAS Registry Number.

881652-47-7Downstream Products

881652-47-7Relevant academic research and scientific papers

Synthesis of Sultams and Cyclic N-Sulfonyl Ketimines via Iron-Catalyzed Intramolecular Aliphatic C-H Amidation

Zhong, Dayou,Wu, Di,Zhang, Yan,Lu, Zhiwu,Usman, Muhammad,Liu, Wei,Lu, Xiuqiang,Liu, Wen-Bo

, p. 5808 - 5812 (2019/08/26)

Cyclic sulfonamides (sultams) play a unique role in drug discovery and synthetic chemistry. A direct synthesis of sultams by an intramolecular C(sp3)-H amidation reaction using an iron complex in situ derived from Fe(ClO4)2 and aminopyridine ligand is reported. This strategy features a readily available catalyst and tolerates a broad variety of substrates as demonstrated by 22 examples (up to 89% yield). A one-pot iron-catalyzed amidation/oxidation procedure for the synthesis of cyclic N-sulfonyl ketimines is also realized with up to 92% yield (eight examples). The synthetic utility of the method is validated by a gram-scale reaction and derivatization of the products to ring-fused sultams.

Sultam compound and preparation method thereof

-

Paragraph 0167-0172, (2019/11/12)

The invention provides a sultam compound and a preparation method thereof. The method provided by the invention specifically comprises the following steps: putting a catalyst C, sulfamide B and an oxidant D into an organic solvent, performing a reaction,

Formal palladium-catalyzed asymmetric hydrogenolysis of racemic N -sulfonyloxaziridines

Song, Bo,Yu, Chang-Bin,Huang, Wen-Xue,Chen, Mu-Wang,Zhou, Yong-Gui

supporting information, p. 190 - 193 (2015/01/30)

Highly enantioselective palladium-catalyzed formal hydrogenolysis of racemic N-sulfonyloxaziridines has been realized, providing a novel access to sultams with up to 99% ee. Preliminary mechanistic insights revealed that the reaction proceeded through a N-O bond cleavage, dehydration, and the sequential asymmetric hydrogenation.

A synthesis of novel N-sulfonylated β-amino acids

Freitag, Dirk,Metz, Peter

, p. 1799 - 1805 (2007/10/03)

Novel N-sulfonyl β-amino acids were efficiently prepared in a seven-step synthesis starting from Boc protected methanesulfonamide and terminal epoxides. A zinc-mediated allylation of cyclic N-sulfonyl imines readily derived from these building blocks serv

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