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1-(benzylsulfonyl)-3-fluorobenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1204677-76-8

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1204677-76-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1204677-76-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,4,6,7 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1204677-76:
(9*1)+(8*2)+(7*0)+(6*4)+(5*6)+(4*7)+(3*7)+(2*7)+(1*6)=148
148 % 10 = 8
So 1204677-76-8 is a valid CAS Registry Number.

1204677-76-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(benzylsulfonyl)-3-fluorobenzene

1.2 Other means of identification

Product number -
Other names .benzyl(3-fluorophenyl)sulfane

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:1204677-76-8 SDS

1204677-76-8Relevant academic research and scientific papers

Synthesis of alcohols from m-fluorophenylsulfones and dialkylboranes: Application to the C14-C35 building block of E7389

Liu, Lei,Henderson, James A.,Yamamoto, Akihiko,Bremond, Paul,Kishi, Yoshito

experimental part, p. 2262 - 2265 (2012/06/30)

The reaction of m-fluorophenylsulfone anions with dialkylboranes, followed by alkaline hydroperoxide oxidation, yields alcohols in high yields. Optimization of the process, scope and limitation, and application to the synthesis of one of the C14-C35 building blocks of E7389, a right half analogue of halichondrin B, are reported.

Iodine-mediated thioetherification of alcohols with disulfides or NaSh under microwave irradiation

Hu, Bolun,Sun, Leilei,Tang, Riyuan,Hu, Huanan

, p. 2556 - 2562,7 (2020/09/16)

An efficient and novel method for the thioetherification of an alcohol with disulfides or NaSH under microwave irradiation is presented. In the presence of iodine, a variety of alcohols were smoothly S-alkylated with disulfides or NaSH to give the corresponding thioethers in moderate to excellent yields. Copyright

Regioselective C-S bond formation accomplished by copper-catalyzed regioselective C-F substitution of perfluoroarenes with aryl thioacetates or benzyl thioacetate

Zhou, Qizhong,Zhang, Bin,Du, Tieqi,Gu, Haining,Jiang, Huajiang,Chen, Rener

experimental part, p. 4233 - 4241 (2012/07/14)

Practical and straightforward method for regioselective C-S bond formation accomplished by copper-catalyzed regioselective C-F substitution of electron-deficient perfluoroarenes with aryl thioacetates or benzyl thioacetate has been developed. Because of its high reaction efficiency, good chemoselectivity and regioselectivity, and excellent functional-group compatibility, this protocol provides a useful and operationally simple access to polyfluoroaryl thioethers used for drugs and material chemistry.

A novel and efficient cross-coupling of tris(fluorinated phenyl)boroxins with disulfides catalyzed by CuI/1,10-phenanthroline

Yu, Chuanming,Jin, Beibei,Liu, Zhenyu,Zhong, Weihui

experimental part, p. 485 - 491 (2010/09/17)

Under an oxygen atmosphere, the cross-coupling of tris(fluorinated phenyl)boroxins and disulfides catalyzed by CuI/1,10-phenanthroline were smoothly achieved to produce the corresponding asymmetric fluorinated arylsulfides in good-to-excellent yields.

Synthesis of aryl benzyl NH-sulfoximines

Barry, Nicola,Brondel, Nicolas,Lawrence, Simon E.,Maguire, Anita R.

experimental part, p. 10660 - 10670 (2010/01/16)

Efficient synthesis and characterisation of a series of aryl benzyl NH-sulfoximines are described. While N-protected versions of aryl benzyl sulfoximines have been previously described, reports of their deprotection are very limited, presumably due to lab

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