130890-90-3 Usage
Uses
Used in Pharmaceutical Industry:
Benzene, 1-fluoro-3-[(phenylsulfonyl)methyl]is used as a building block for the synthesis of various pharmaceuticals, contributing to the development of new drugs and improving existing ones.
Used in Agrochemical Industry:
Benzene, 1-fluoro-3-[(phenylsulfonyl)methyl]is also utilized as a building block in the synthesis of agrochemicals, playing a role in the creation of pesticides and other agricultural products to enhance crop protection and yield.
Used as a Reagent in Chemical Reactions:
Benzene, 1-fluoro-3-[(phenylsulfonyl)methyl]serves as a reagent in various chemical reactions, facilitating the formation of desired products and aiding in the advancement of chemical research and development.
Used as a Starting Material for Organic Compounds:
It is employed as a starting material for the preparation of a range of organic compounds, expanding the scope of organic synthesis and contributing to the discovery of new chemical entities.
Note: Due to its potential health hazards, including its carcinogenic properties, proper handling and safety precautions are essential when working with Benzene, 1-fluoro-3-[(phenylsulfonyl)methyl]-.
Check Digit Verification of cas no
The CAS Registry Mumber 130890-90-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,8,9 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 130890-90:
(8*1)+(7*3)+(6*0)+(5*8)+(4*9)+(3*0)+(2*9)+(1*0)=123
123 % 10 = 3
So 130890-90-3 is a valid CAS Registry Number.
130890-90-3Relevant academic research and scientific papers
Palladium-catalyzed Negishi α-arylation of alkylsulfones
Zhou, Gang,Ting, Pauline C.,Aslanian, Robert G.
experimental part, p. 939 - 941 (2010/05/18)
A general, mild catalytic system for α-monoarylation of various alkyl sulfones is described that utilizes palladium-catalyzed Negishi cross-coupling approach.
Novel synthesis of sulfones from α,α-dibromomethyl aromatics
Xu, Feng,Savary, Kimberly,Williams, J. Michael,Grabowski, Edward J. J.,Reider, Paul J.
, p. 1283 - 1286 (2007/10/03)
A novel, high yielding preparation of sulfones from α,α-dibromomethyl aromatics through reaction with a sulfinate salt is reported.
