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1889-59-4

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1889-59-4 Usage

Chemical Properties

clear yellow liquid

General Description

Ethly vinyl sulfone alkylates ε-amino groups of lysine side chains and imidazole groups of histidine residues in proteins. Chemical modification of bovine serum albumin by ethyl vinyl sulfone has been studied by X-ray photoelectron spectroscopy.

Check Digit Verification of cas no

The CAS Registry Mumber 1889-59-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,8 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1889-59:
(6*1)+(5*8)+(4*8)+(3*9)+(2*5)+(1*9)=124
124 % 10 = 4
So 1889-59-4 is a valid CAS Registry Number.
InChI:InChI=1/C4H8O2S/c1-3-7(5,6)4-2/h3H,1,4H2,2H3

1889-59-4 Well-known Company Product Price

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  • Aldrich

  • (282839)  Ethylvinylsulfone  98%

  • 1889-59-4

  • 282839-5G

  • 601.38CNY

  • Detail

1889-59-4SDS

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 1-ethenylsulfonylethane

1.2 Other means of identification

Product number -
Other names 1-(ethylsulfonyl)ethene

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:1889-59-4 SDS

1889-59-4Relevant articles and documents

-

Sayigh,A.A.R. et al.

, p. 2042 - 2043 (1964)

-

Mo(VI) complex catalysed synthesis of sulfonees and their modification for anti-HIV activities

Madduluri, Vimal Kumar,Baig, Noorullah,Chander, Subhash,Murugesan, Sankaranarayanan,Sah, Ajay K.

, (2020/01/23)

An efficient method for the synthesis of sulfones has been developed using sugar derived cis-dioxo molybdenum(VI) complex as catalyst and urea hydrogen peroxide as oxygen source. Present method is highly specific for sulfide oxidation irrespective of presence of alkene and aldehyde groups in the same molecule. Synthesis of fifteen sulfones have been reported with 82–98% isolated yields and the catalyst has been reused five times without any loss in its activity. 2-(Phenylsulfonyl)aniline has been condensed with eight different aromatic aldehydes and the products are being explored for HIV-1 reverse transcriptase inhibition activities.

Difluoro- and trifluoro diazoalkanes-complementary approaches in batch and flow and their application in cycloaddition reactions

Hock, Katharina J.,Mertens, Lucas,Metze, Friederike K.,Schmittmann, Clemens,Koenigs, Rene M.

supporting information, p. 905 - 909 (2017/08/14)

Herein we report on applications of fluorinated diazoalkanes in cycloaddition reactions, with the emphasis on studying subtle differences between diverse fluorinated diazo compounds. These differences led to two major synthetic protocols in batch and flow that allow the safe and scalable synthesis of fluoroalkyl-, sulfone-substituted pyrazolines.

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