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4-methyl-N-(2-(oxiran-2-yl)ethyl)benzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1369589-59-2

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1369589-59-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1369589-59-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,9,5,8 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1369589-59:
(9*1)+(8*3)+(7*6)+(6*9)+(5*5)+(4*8)+(3*9)+(2*5)+(1*9)=232
232 % 10 = 2
So 1369589-59-2 is a valid CAS Registry Number.

1369589-59-2Downstream Products

1369589-59-2Relevant academic research and scientific papers

M-CPBA-Mediated Intramolecular Aminohydroxylation of N-Sulfonyl Aminoalkenes to Synthesize β-Hydroxyl Cyclic Amines

Yin, Yan,Zhou, Hong,Sun, Guofeng,Liu, Xichen

, p. 1337 - 1345 (2015)

A variety of structurally diverse N-sulfonyl-protected aminoalkenes readily reacted with m-CPBA to produce a series of β-hydroxyl cyclic amines in high yields through intramolecular aminohydroxylation. This metal-free and easy-to-handle synthetic methodol

[5+2] Cycloaddition of 2-(2-Aminoethyl)oxiranes with Alkynes via Epoxide Ring-Opening: A Facile Access to Azepines

Hu, Chao,Song, Ren-Jie,Hu, Ming,Yang, Yuan,Li, Jin-Heng,Luo, Shenglian

, p. 10423 - 10426 (2016/08/24)

A new FeCl3and BF3?OEt2co-catalyzed tandem hetero-[5+2] cycloaddition of 2-(2-aminoethyl)oxiranes with a wide range of alkynes, including terminal alkynes and alkyl-substituted internal alkynes is presented. This is the fi

Hf(IV)-catalyzed enantioselective epoxidation of N-alkenyl sulfonamides and N-tosyl imines

Olivares-Romero, Jose Luis,Li, Zhi,Yamamoto, Hisashi

supporting information; experimental part, p. 5440 - 5443 (2012/05/20)

Asymmetric epoxidation of allylic and homoallylic amine derivatives catalyzed by Hf(IV)-bishydroxamic acid complexes is described. Under similar conditions, aldimine and ketimine produced oxaziridines. The sulfonyl group is demonstrated to be an effective directing group for these transformations.

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