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(2S,3S)-3-hydroxy-2-(4-methoxyphenyl)-2,3-dihydrobenzo[b][1,4]thiazepin-4(5H)-one 1-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

137447-97-3

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137447-97-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 137447-97-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,4,4 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 137447-97:
(8*1)+(7*3)+(6*7)+(5*4)+(4*4)+(3*7)+(2*9)+(1*7)=153
153 % 10 = 3
So 137447-97-3 is a valid CAS Registry Number.

137447-97-3Downstream Products

137447-97-3Relevant academic research and scientific papers

New Chiral Solvating Agents: 1,5-Benzothiazepines

Giordano, Claudio,Restelli, Angelo

, p. 785 - 788 (1991)

For the first time it is reported that 1,5-benzothiazepines (1a-e) (Figure 1) behave as effective chiral solvating agents (CSA) for NMR enantiomeric excess (ee) determination of different classes of compounds such as α-arylalkanoic acids, α-hydroxy acids,

Metal- and additive-free oxygen-atom transfer reaction: an efficient and chemoselective oxidation of sulfides to sulfoxides with cyclic diacyl peroxides

Gan, Shaoyan,Yin, Junjie,Yao, Yuan,Liu, Yang,Chang, Denghu,Zhu, Dan,Shi, Lei

supporting information, p. 2647 - 2654 (2017/04/03)

Metal- and additive-free oxidation of a series of sulfides/thioketones has been achieved using cyclic diacyl peroxides as mild oxygen sources. This protocol features simple manipulation, high chemo- and diastereoselectivity, and a broad substrate scope (up to 42 examples), tolerates many common functional groups, and is scalable and applicable to the late-stage sulfoxidation strategy. A preliminary mechanistic study by quantum mechanical calculations suggests that a single two-electron transfer process is energetically more favorable, and indicates the reactivity of cyclic diacyl peroxides distinct from conventional acyclic acyl peroxides.

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