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Benzene, [(ethylsulfonyl)ethynyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

33987-87-0

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33987-87-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33987-87-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,9,8 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 33987-87:
(7*3)+(6*3)+(5*9)+(4*8)+(3*7)+(2*8)+(1*7)=160
160 % 10 = 0
So 33987-87-0 is a valid CAS Registry Number.

33987-87-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-ethanesulfonylethynyl)benzene

1.2 Other means of identification

Product number -
Other names Ethyl-phenylethinyl-sulfon

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:33987-87-0 SDS

33987-87-0Downstream Products

33987-87-0Relevant academic research and scientific papers

Radical-mediated sulfonyl alkynylation, allylation, and cyanation of propellane

Wu, Zhen,Xu, Yaohui,Zhang, Huihui,Wu, Xinxin,Zhu, Chen

supporting information, p. 6066 - 6069 (2021/06/21)

Bicyclo[1.1.1]pentane (BCP) is widely applied as the bioisostere for aryl, internal alkynes, andtert-butyl groups in medicinal chemistry. We herein disclose an efficient and practical preparation of sulfonyl alkynyl/allyl/cyano-substituted BCP derivatives

Method for synthesizing aryl acetylene alkyl sulfone compounds based on alkyl fluoroborate

-

Paragraph 0035-0036, (2020/02/14)

The invention belongs to the technical field of organic chemistry and in particular relates to a method for synthesizing aryl acetylene alkyl sulfone compounds based on alkyl fluoroborate. The methodfor synthesizing the aryl acetylene alkyl sulfone compounds, which is provided by the invention, comprises the following steps: under a condition of visible light, exciting a photosensitizer 9-symtrimethophenyl-10-methyl acridine perchlorate (Mes-AcrClO4, CAS: 674783-97-2), further enabling the photosensitizer to act on potassium alkyl fluoroborate so as to obtain an alkyl free radical, combining the alkyl free radical with sulfur dioxide to generate an alkyl sulfonyl free radical, and performing addition on the alkyl sulfonyl free radical with aryl acetylene bromide, so as to obtain a series of aryl acetylene alkyl sulfone compounds. The preparation method of the aryl acetylene alkyl sulfone compounds, which is provided by the invention, is mild in condition, simple and efficient, high in reaction yield, high in product purity and very convenient in separation and purification, and has very good application values.

Ruthenium-catalyzed [2+2] cycloadditions of alkynyl sulfides and alkynyl sulfones

Riddell, Nicole,Tam, William

, p. 1934 - 1937 (2007/10/03)

Ruthenium-catalyzed [2+2] cycloadditions of bicyclic alkenes with alkynyl sulfides and alkynyl sulfones were investigated. The sulfide and sulfone moieties were found to be compatible with the Ru-catalyzed cycloadditions, giving the corresponding cyclobut

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