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2-Propenoic acid, 3-(phenylsulfonyl)-, (Z)-, also known as (Z)-3-(phenylsulfonyl)acrylic acid, is an organic compound characterized by a unique molecular structure. It features a phenylsulfonyl group attached to the third carbon of the acrylic acid backbone, with the double bond existing between the second and third carbon atoms, giving it a (Z)-configuration. 2-Propenoic acid, 3-(phenylsulfonyl)-, (Z)- is significant in organic chemistry, particularly in the synthesis of various pharmaceuticals and agrochemicals, due to its reactive functional groups and potential to form conjugated systems. It is also known for its potential applications in the preparation of sulfonamide derivatives, which have broad utility in the chemical industry.

711-30-8

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711-30-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 711-30-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 711-30:
(5*7)+(4*1)+(3*1)+(2*3)+(1*0)=48
48 % 10 = 8
So 711-30-8 is a valid CAS Registry Number.

711-30-8SDS

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 Z-3-phenylsulfonylacrylic acid

1.2 Other means of identification

Product number -
Other names 3c-benzenesulfonyl-acrylic acid

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:711-30-8 SDS

711-30-8Downstream Products

711-30-8Relevant academic research and scientific papers

Lipase-catalyzed asymmetric synthesis of naphtho[2,3-c]furan-1(3H)-one derivatives by a one-pot dynamic kinetic resolution/intramolecular Diels–Alder reaction: Total synthesis of (?)-himbacine

Sugiyama, Koji,Kawanishi, Shinji,Oki, Yasuhiro,Kamiya, Marin,Hanada, Ryosuke,Egi, Masahiro,Akai, Shuji

supporting information, p. 1378 - 1386 (2017/10/06)

One-pot sequential reactions using the acyl moieties installed by enzymatic dynamic kinetic resolution of alcohols have been little investigated. In this work, the acryloyl moiety installed via the lipase/oxovanadium combo-catalyzed dynamic kinetic resolution of a racemic dienol [4-(cyclohex-1-en-1-yl)but-3-en-2-ol or 1-(cyclohex-1-en-1-yl)but-2-en-1-ol] with a (Z)-3-(phenylsulfonyl)acrylate underwent an intramolecular Diels–Alder reaction in a one-pot procedure to produce an optically active naphtho[2,3-c]furan-1(3H)-one derivative (98% ee). This method was successfully applied to the asymmetric total synthesis of (?)-himbacine.

A Mild, Inexpensive and Practical Oxidation of Sulfides

Webb, Kevin S.

, p. 3457 - 3460 (2007/10/02)

Several sulfides have been converted to sulfoxides or sulfones in modest to excellent yields.The oxidant was oxone and the reactions were performed in 12.5percent aqueous acetone and buffered to pH 7.5-8.0 with sodium bicarbonate.

Pharmaceutical compositions containing acrylic acid derivatives and their use in the medicine

-

, (2008/06/13)

Known acrylic acid derivatives of formula wherein, n is an integer of from 0 to 2,R represents a hydrogen, an alkaline or an alkaline earth metal atom, or a C1 4alkyl-group, and, R1 represents a hydrogen or a halogen atom or a C

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