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

140666-28-0

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140666-28-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 140666-28-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,6,6 and 6 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 140666-28:
(8*1)+(7*4)+(6*0)+(5*6)+(4*6)+(3*6)+(2*2)+(1*8)=120
120 % 10 = 0
So 140666-28-0 is a valid CAS Registry Number.

140666-28-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-iodophenyl)-4-methyl-N-(prop-2-ynyl)benzenesulfonamide

1.2 Other means of identification

Product number -
Other names N-(2-iodophenyl)-N-2-propynyl-p-tolylsulfonamide

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:140666-28-0 SDS

140666-28-0Relevant academic research and scientific papers

Palladium-Catalyzed Allenamide Carbopalladation/Allylation with Active Methine Compounds

Zhu, Xiaoyi,Li, Ruibo,Yao, Hequan,Lin, Aijun

, p. 4630 - 4634 (2021/06/28)

A palladium-catalyzed allenamide carbopalladation/allylation with active methine compounds has been developed. Various indoles and isoquinolinones bearing a quaternary carbon center were achieved with good efficiency, a broad substrate scope and good functional group tolerance. This reaction underwent cascade oxidative addition, carbopalladation, and allylic alkylation, and two new C-C bonds were formed in one pot.

Indole acetyl imino sulfone series compound and preparation method thereof

-

Paragraph 0030; 0034-0098, (2021/07/28)

The invention provides an indole acetyl imino sulfone series compound and a preparation method thereof. According to the preparation method, by taking ortho-halogen substituted arylamine, propargyl halide and sulfoxide sulfimide as reaction substrates, re

Asymmetric Domino Heck/Dearomatization Reaction of β-Naphthols to Construct Indole-Terpenoid Frameworks

Wang, Dong-Chao,Cheng, Peng-Peng,Yang, Ting-Ting,Wu, Pan-Pan,Qu, Gui-Rong,Guo, Hai-Ming

supporting information, p. 7865 - 7872 (2021/10/20)

A palladium-catalyzed enantioselective Heck cyclization/dearomatization cascade via capturing the cyclized Heck π-allylpalladium intermediate by β-naphthols is reported, which provides a new strategy for the construction of chiral indole-terpenoid framewo

Tris(trimethylsilyl)silane and visible-light irradiation: A new metal- and additive-free photochemical process for the synthesis of indoles and oxindoles

Da Silva, Gustavo Piva,Ali, Akbar,Da Silva, Rodrigo César,Jiang, Hao,Paix?o, Márcio W.

, p. 15110 - 15113 (2015/10/12)

A combined tris(trimethylsilyl)silane and visible-light-promoted intramolecular reductive cyclization protocol for the synthesis of indoles and oxindoles has been developed. This straightforward and efficient method shows tolerance towards a broad spectru

An approach to cyclohepta[ b ]indoles through an allenamide (4 + 3) cycloaddition-grignard cyclization-chugaev elimination sequence

He, Shuzhong,Hsung, Richard P.,Presser, William R.,Ma, Zhi-Xiong,Haugen, Bryan J.

, p. 2180 - 2183 (2014/05/06)

A strategy for synthesizing highly functionalized cyclohepta[b]indoles through a concise (4 + 3) cycloaddition-cyclization-elimination sequence is described. The cycloaddition features nitrogen-stabilized oxyallyl cations derived from epoxidations of N-ar

Carbolithiation of chloro-substituted alkynes: A new access to vinyl carbenoids

Lhermet, Rudy,Ahmad, Maha,Fressigne, Catherine,Silvi, Bernard,Durandetti, Muriel,Maddaluno, Jacques

, p. 10249 - 10254 (2014/08/18)

The intramolecular carbolithiation of a series of chloro-substituted alkynes leads to exocyclic alkylidene carbenoids of which both nucleophilic and electrophilic characters can be drove. A sole stereoselective 5-exo-dig addition takes place, probably bec

A strategy for the synthesis of 2,3-disubstituted indoles starting from N-(o-halophenyl)allenamides

Fuwa, Haruhiko,Sasaki, Makoto

, p. 2214 - 2218 (2008/03/14)

A strategy for the synthesis of 2,3-disubstituted indole derivatives based on an intramolecular carbopalladation-anion capture cascade has been developed, wherein construction of the pyrrole ring and functionalisation of the indole C2 and C3 positions wer

CONVERSION OF 2-IODOANILINE INTO (Z)-3-METHYLENE-2,3-DIHYDROINDOLE DERIVATIVES

Luo, Fen-Tair,Wang, Ren-Tzong

, p. 2365 - 2372 (2007/10/02)

Treatment of N-(2-iodophenyl)-N-2-propynyl-p-tolylsulfonamide with various organozinc chlorides in the presence of palladium acetate, triphenylphosphine, and 1 equiv. of triethylamine in tetrahydrofuran gives (Z)-3-alkylidene-2,3-dihydroindoles via intramolecular Heck-type reaction and successive cross coupling reactions.

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