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

697287-96-0

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697287-96-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 697287-96-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,7,2,8 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 697287-96:
(8*6)+(7*9)+(6*7)+(5*2)+(4*8)+(3*7)+(2*9)+(1*6)=240
240 % 10 = 0
So 697287-96-0 is a valid CAS Registry Number.

697287-96-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-N-(2-oxo-2-phenylethyl)-N-(prop-2-yn-1-yl)benzenesulfonamide

1.2 Other means of identification

Product number -
Other names N-(2-phenyl-2-oxoethyl)-N-2-propynyltosylamide

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:697287-96-0 SDS

697287-96-0Relevant academic research and scientific papers

Ni/AntPohs-Catalyzed Stereoselective Asymmetric Intramolecular Reductive Coupling of N-1,6-Alkynones

Chen, Wanjun,Cheng, Yaping,Zhang, Tao,Mu, Yu,Jia, Wenqi,Liu, Guodu

, p. 5166 - 5182 (2021/05/05)

An efficient nickel-catalyzed stereoselective asymmetric intramolecular reductive coupling of N-1,6-alkynones is reported. A P-chiral monophosphine ligand AntPhos was found to be a privileged catalyst for constructing versatile functionalized chiral pyrro

Thiyl radical-mediated cyclization of ω-alkynyl O-tert-butyldiphenylsilyloximes

Shibata, Nina,Tsuchiya, Takahisa,Hashimoto, Yoshimitsu,Morita, Nobuyoshi,Ban, Shintaro,Tamura, Osamu

supporting information, p. 3025 - 3034 (2017/04/10)

ω-Alkynyl O-tert-butyldiphenylsilyloximes, upon treatment with odorless 4-tert-butylbenzenethiol in the presence of azobisisobutyronitrile (AIBN) in refluxing benzene, underwent addition of a thiyl radical to the alkynyl group followed by radical cyclizat

Vinyl dihydropyrans and dihydrooxazines: Cyclizations of catalytic ruthenium carbenes derived from alkynals and alkynones

Cambeiro, Fermin,Lopez, Susana,Varela, Jesus A.,Saa, Carlos

, p. 5959 - 5963 (2014/06/10)

A novel synthesis of 2-vinyldihydropyrans and dihydro-1,4-oxazines (morpholine derivatives) from alkynals and alkynones has been developed. The cyclizations require a mild generation of catalytic ruthenium carbenes from terminal alkynes and (trimethylsilyl)diazomethane followed by trapping with carbonyl nucleophiles. Mechanistic aspects of the new cyclizations are discussed. Setting a trap: A novel synthesis of 2-vinyldihydropyrans and dihydro-1,4-oxazines (morpholine derivatives) from alkynals and alkynones has been developed. The cyclizations require a mild generation of catalytic ruthenium carbenes from terminal alkynes and (trimethylsilyl)diazomethane followed by trapping with carbonyl nucleophiles.

Silver(I)-Catalyzed conia-ene reaction: Synthesis of 3-pyrrolines via a 5-endo-dig cyclization

Boominathan, Siva Senthil Kumar,Hu, Wan-Ping,Senadi, Gopal Chandru,Wang, Jeh-Jeng

, p. 3570 - 3574 (2014/01/06)

A novel method has been developed for the synthesis of 3-pyrrolines from β-ketopropargylamines via a 5-endo-dig carbocyclization. This transformation involves a silver-catalyzed Conia-ene type reaction tolerating broad substrate scope with good to excellent yields. Furthermore, this methodology has been extended for the construction of 2-substituted pyrroles under base-mediated conditions. Copyright

Investigation of intramolecular Pauson-Khand reaction of 2-aryl-1,6- and 1-methyl-1,7-enynes (exo-olefins) and 1-phenyl-1-octen-7-yne (endoolefin)

Ishizaki, Miyuki,Satoh, Hiroshi,Hoshino, Osamu,Nishitani, Kiyoshi,Hara, Hiroshi

, p. 827 - 844 (2007/10/03)

The intramolecular Pauson-Khand reaction of various 2-aryl-1-hepten-6-ynes and its aza-derivatives (exo-olefins) efficiently produced arylbicyclo[3.3.0]octenones and azaoctenone bearing quaternary carbon centers at angular positions in good yields. Although a similar reaction of 2-phenyl-1-octen-7-yne (exo-olefin), which is a homologue of 2-phenyl-1-hepten-6-yne, did not take place, the reaction of the methyl derivatives smoothly proceeded. However, the reaction of regioisomeric 1-phenyl-1-octen-7-yne (endo-olefin) afforded the desired product in moderate yields.

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