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Benzenesulfonamide, 2-(2-propenyl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

291514-04-0

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291514-04-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 291514-04-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,1,5,1 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 291514-04:
(8*2)+(7*9)+(6*1)+(5*5)+(4*1)+(3*4)+(2*0)+(1*4)=130
130 % 10 = 0
So 291514-04-0 is a valid CAS Registry Number.

291514-04-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-prop-2-enylbenzenesulfonamide

1.2 Other means of identification

Product number -
Other names 2-allybenzenesulfonamide

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:291514-04-0 SDS

291514-04-0Relevant articles and documents

Design and synthesis of cyclic sulfonamides and sulfamates as new calcium sensing receptor agonists

Kiefer, Lionel,Gorojankina, Tatiana,Dauban, Philippe,Faure, Hélène,Ruat, Martial,Dodd, Robert H.

scheme or table, p. 7483 - 7487 (2011/02/21)

The design, synthesis and calcimimetic properties of various cyclic sulfonamides and sulfamates are described. The latter were prepared from the corresponding o-alkenylarenesulfonamides via copper- or rhodium-catalyzed intramolecular aziridination. The si

Efficient aziridination of olefins catalyzed by dirhodium catalysts

-

Page/Page column 13, (2010/11/23)

This invention relates to compositions and methods for achieving the efficient aziridination of organic molecules, especially olefins. More specifically, the invention is directed to a mild, selective, and efficient aziridination protocol that involves catalysis by a mixed-valent dirhodium(II,III) catalyst (Rh25+). Especially preferred sources for forming such mixed-valent dirhodium(II,III) catalyst (Rh25+) are dirhodium(II) carboxamidates, such as dirhodium(II) caprolactamate, and their derivatives and analogues.

Modulators of serotonin receptors

-

Page/Page column 74, (2010/02/11)

The present invention provides modulators of serotonin receptors, pharmaceutical compositions containing such modulators and methods for treating various diseases, conditions and disorders associated with modulation of serotonin receptors such as, for exa

Rhodium(II)-catalyzed aziridination of allyl-substituted sulfonamides and carbamates

Padwa, Albert,Flick, Andrew C.,Leverett, Carolyn A.,Stengel, Thomas

, p. 6377 - 6386 (2007/10/03)

Several unsaturated sulfonamides underwent intramolecular aziridination when treated with PhI-(OAc)2, MgO, and catalytic Rh 2(OAc)4 to give bicyclic aziridines in excellent yield. Treatment of the resulting azabicyclic sul

Synthesis of cyclic sulfonamides via intramolecular copper-catalyzed reaction of unsaturated iminoiodinanes

Dauban, Philippe,Dodd, Robert H.

, p. 2327 - 2329 (2007/10/03)

(equation presented) Olefinic primary sulfonamides were treated with iodebenzene diacetate and potassium hydroxide in methanol to give intermediate iminoiodinanes. Catalytic copper(I) or (II) triflate then provided intramolecular nitrene delivery leading to aziridene formation except in one case where a rare copper-catalyzed C-H insertion was observed. The aziridines could be opened by various nucleophiles (methanol, thiophenol, allylmagnesium bromide, benzylamine) to give the corresponding substituted cyclic sulfonamides.

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