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89654-30-8

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89654-30-8 Usage

Description

[(2-phenylcyclopropyl)sulfonyl]benzene is a chemical compound characterized by the molecular formula C18H16O2S. It is a white solid that is insoluble in water and is known for its unique properties and reactivity due to the presence of a sulfonyl group attached to a phenylcyclopropyl ring. [(2-phenylcyclopropyl)sulfonyl]benzene is primarily utilized in organic synthesis and serves as a valuable building block in the field of organic chemistry.

Uses

Used in Pharmaceutical Synthesis:
[(2-phenylcyclopropyl)sulfonyl]benzene is used as a reactive intermediate for the synthesis of various pharmaceuticals. Its sulfonyl group, being a strong electron-withdrawing group, contributes to its utility in chemical reactions, making it a crucial component in the development of new drugs.
Used in Agrochemical Synthesis:
Similarly, in the agrochemical industry, [(2-phenylcyclopropyl)sulfonyl]benzene is employed as a key intermediate in the synthesis of different agrochemicals. Its unique structure and properties enable the creation of novel compounds with potential applications in agriculture.
Used in Organic Chemistry Research:
[(2-phenylcyclopropyl)sulfonyl]benzene is also used as a building block in organic chemistry research. Its distinct properties make it an interesting subject for studying various chemical reactions and exploring new synthetic pathways. This contributes to the advancement of knowledge in organic chemistry and the development of innovative chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 89654-30-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,6,5 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 89654-30:
(7*8)+(6*9)+(5*6)+(4*5)+(3*4)+(2*3)+(1*0)=178
178 % 10 = 8
So 89654-30-8 is a valid CAS Registry Number.

89654-30-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-(benzenesulfonyl)cyclopropyl]benzene

1.2 Other means of identification

Product number -
Other names Benzene,cis

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:89654-30-8 SDS

89654-30-8Downstream Products

89654-30-8Relevant articles and documents

Synthesis of substituted tetrahydrofurans via intermolecular reactions of γ-chlorocarbanions of 3-substituted 3-chloro-propylphenyl sulfones with aldehydes

Brandt, Agnieszka,Wojtasiewicz, Anna,?niezek, Marcin,Makosza, Mieczys?aw

experimental part, p. 3378 - 3385 (2010/06/20)

Carbanions of 3-substituted-3-chloropropyl phenyl sulfones add to carbonyl groups of aldehydes to produce aldol type adducts that undergo 1,5-intramolecular substitution giving 2,3,5-trisubstituted tetrahydrofurans. The effect of substituents in the 3-pos

Improved dimethylsulfoxonium methylide cyclopropanation procedures, including a tandem oxidation variant

Paxton, Richard J.,Taylor, Richard J. K.

, p. 633 - 637 (2007/10/03)

A new procedure for the cyclopropanation of α,β-unsaturated carbonyl compounds and related systems is described which employs trimethylsulfoxonium iodide and an organic base in acetonitile to generate dimethylsulfoxonium methylide in situ; in addition, pr

Phase transfer catalyzed cyclopropanation of trans-styryl aryl sulfones with dimethyl sulfoxonium methylide

Padmaja,Ramachandra Reddy,Subba Reddy,Bhaskar Reddy

, p. 91 - 98 (2007/10/03)

Some new trans-aryl cyclopropyl sulfones (II) have been prepared by the cycloaddition of dimethylsulfoxonium methylide to trans-styryl aryl sulfones (I) by two different methods. It is observed that the reaction in presence of a phase transfer catalyst proceeds in a facile manner.

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