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Benzenesulfonamide, 4-methyl-N-(2-methylpropylidene)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

353264-99-0

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353264-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 353264-99-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,3,2,6 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 353264-99:
(8*3)+(7*5)+(6*3)+(5*2)+(4*6)+(3*4)+(2*9)+(1*9)=150
150 % 10 = 0
So 353264-99-0 is a valid CAS Registry Number.

353264-99-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-N-(2-methylpropylidene)benzenesulfonamide

1.2 Other means of identification

Product number -
Other names N-isobutylidene-p-methyl-benzenesulfonamide

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:353264-99-0 SDS

353264-99-0Relevant academic research and scientific papers

Alkenyl Exchange of Allylamines via Nickel(0)-Catalyzed C-C Bond Cleavage

Fan, Chao,Lv, Xin-Yang,Xiao, Li-Jun,Xie, Jian-Hua,Zhou, Qi-Lin

, p. 2889 - 2893 (2019/02/19)

A functional group exchange reaction between allylamines and alkenes via nickel-catalyzed C - C bond cleavage and formation was developed. This reaction provides a novel protocol, which does not require the use of unstable imine substrates, for the synthesis of allylamines, which are widely used in the production of fine chemicals, pharmaceuticals, and agrochemicals.

Synthesis of Benzyl Amines via Copper-Catalyzed Enantioselective Aza-Friedel-Crafts Addition of Phenols to N -Sulfonyl Aldimines

Shikora, Jonathan M.,Chemler, Sherry R.

supporting information, p. 2133 - 2137 (2018/04/30)

A new copper-catalyzed enantioselective aza-Freidel-Crafts reaction between phenols and N-sulfonyl aldimines that provides chiral secondary benzylamines in good to excellent yields and excellent enantioselectivities (up to 99% ee) is disclosed. In particular, excellent scope with alkylimines was observed for the first time. The synthetic utility of the products was demonstrated in the first enantioselective synthesis of a dual orexin receptor antagonist, a compound that contains an amine-bearing stereocenter adjacent to a bis-ortho-functionalized arene.

Nickel(0)-Catalyzed Hydroalkenylation of Imines with Styrene and Its Derivatives

Xiao, Li-Jun,Zhao, Chao-Yue,Cheng, Lei,Feng, Bo-Ya,Feng, Wei-Min,Xie, Jian-Hua,Xu, Xiu-Fang,Zhou, Qi-Lin

, p. 3396 - 3400 (2018/03/01)

A nickel(0)-catalyzed hydroalkenylation of imines with styrene and its derivatives is described. A wide range of aromatic and aliphatic imines directly coupled with styrene and its derivatives, thus providing various synthetically useful allylic amines with up to 95 % yield. The reaction offers a new atom- and step-economical approach to allylic amines by using alkenes instead of alkenyl-metallic reagents. Experiments and DFT calculations showed that TsNH2 promotes the proton transfer from the coordinated olefin to the imine, accompanied by a new C?C bond formation.

Rhodium-Catalyzed Enantioselective Arylation of Aliphatic Imines

Kato, Naoya,Shirai, Tomohiko,Yamamoto, Yasunori

supporting information, p. 7739 - 7742 (2016/06/09)

Chiral rhodium(I)-catalyzed highly enantioselective arylation of aliphatic N-sulfonyl aldimines with arylboronic acids has been developed. This transformation is achieved by the use of a rhodium/bis(phosphoramidite) catalyst to give enantiomerically enriched α-branched amines (up to 99 % ee). In addition, this system enables efficient synthesis of (+)-NPS R-568 and Cinacalcet which are calcimimetic agents.

Reduction of sulfonylimines with raney nickel

Ruano, Jose Luis Garca,Fernandez-Salas, Jose A.,Maestro, M. Carmen,Parra, Alejandro

, p. 198 - 207,10 (2020/09/02)

Raney-Ni/EtOH reduction of different N-sulfonylimines provides a new entry for synthesizing sulfonamides in good yields under mild conditions. This protocol, which does not require additional hydrogen, constitutes a cheap, safe, and easy-to-handle alterna

Hydrocyanation of sulfonylimines using potassium hexacyanoferrate(II) as an eco-friendly cyanide source

Li, Zheng,Li, Rongzhi,Zheng, Huanhuan,Wen, Fei,Li, Hongbo,Yin, Junjun,Yang, Jingya

, p. 1739 - 1743 (2014/01/06)

An efficient and eco-friendly method for hydrocyanation of sulfonylimines via one-pot two-step procedure using potassium hexacyanoferrate(II) as a cyanide source, benzoyl chloride as a promoter, and potassium carbonate as a base is described. This protocol has the features of using nontoxic, nonvolatile and inexpensive cyanide source, high yield, and simple work-up procedure.

Dimethylsulfoxide-promoted Strecker reaction of N-tosylaldimines with cyanoformate

Kadam, Santosh T.,Thirupathi, Ponnaboina,Kim, Sung Soo

scheme or table, p. 919 - 923 (2011/05/07)

A metal-free method for performing the Strecker reaction of N-tosylaldimines with ethyl cyanoformate in dimethylsulf-oxide (DMSO) has been developed. Various types of N-tosyl-aldimines undergo the cyanation to provide the N-protected -amino nitriles. This

Highly enantioselective arylation of N -tosylalkylaldimines catalyzed by rhodium-diene complexes

Cui, Zhe,Yu, Hong-Jie,Yang, Rui-Feng,Gao, Wen-Yun,Feng, Chen-Guo,Lin, Guo-Qiang

supporting information; experimental part, p. 12394 - 12397 (2011/10/02)

A highly enantioselective rhodium-catalyzed arylation of aliphatic N-tosylaldimines has been developed. The combination of chiral bicyclo[3.3.0]octadiene ligands, an active rhodium hydroxide complex, and neutral reaction conditions is the key to achieving high yield and enantioselectivity. The application of this method is demonstrated by the enantioselective synthesis of chiral 2-aryl pyrrolidines and piperidines in a one-pot procedure. Furthermore, excellent results are also obtained for the imine substrates with the more readily cleavable N-nosyl protecting group.

Efficient and convenient preparation of N-tosylimines catalyzed by indium trichloride

Deng, Gui Sheng,Zou, Jing Yuan,Sun, Teng Fei

scheme or table, p. 511 - 514 (2012/01/05)

A new method for preparation of N-tosylimines by InCl3-mediated condensation of aldehydes with p-toluenesulfonamide in refluxing benzene is reported. The procedure is lauded by its simplicity, mild reaction conditions, excellent yields and adap

An easy stereoselective access to β,γ-aziridino α-amino ester derivatives via Mannich reaction of benzophenone imines of glycine esters with N-sulfonyl α-chloroaldimines

Kiss, Lorand,Mangelinckx, Sven,Sillanpaeae, Reijo,Fueloep, Ferenc,De Kimpe, Norbert

, p. 7199 - 7206 (2008/02/11)

(Chemical Equation Presented) Mannich-type addition of benzophenone imine glycinates across newly synthesized N-(p-toluenesulfonyl) α- chloroaldimines afforded γ-chloro-α,β-diamino ester derivatives with moderate diastereoselectivity as separable mixtures of anti and syn diastereomers. The γ-chloro-α,β-diamino esters were efficiently cyclized under basic conditions to the corresponding β,γ-aziridino α-amino ester derivatives, representing a new class of conformationally constrained heterocyclic α,β-diamino acid derivatives. The relative configuration of the aziridines was determined via X-ray diffraction analysis. Mechanisms and intermediate transition states to explain the stereochemical outcome of the Mannich reaction with different substrates or under different conditions are proposed. The synthetic importance of the β,γ- aziridino α-amino ester derivatives is demonstrated by their conversion into the corresponding Boc-protected derivatives and ring opening reactions to α,β-diamino esters and a γ-amino α,β-unsaturated amino ester.

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