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339-48-0

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339-48-0 Usage

Physical state

Colorless liquid

Odor

Strong sulfurous

Common uses

Reagent in organic synthesis, leaving group in nucleophilic substitution reactions, protecting group for alcohols in organic chemistry

Hazards

Toxic, potential for skin and eye irritation, should be handled with caution

Check Digit Verification of cas no

The CAS Registry Mumber 339-48-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,3 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 339-48:
(5*3)+(4*3)+(3*9)+(2*4)+(1*8)=70
70 % 10 = 0
So 339-48-0 is a valid CAS Registry Number.

339-48-0SDS

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 2,2,2-trifluoroethyl benzenesulfonate

1.2 Other means of identification

Product number -
Other names benzenesulfonic acid-(2,2,2-trifluoro-ethyl ester)

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:339-48-0 SDS

339-48-0Downstream Products

339-48-0Relevant articles and documents

Nonconventional difluoroalkylation of C(sp2)-H bonds through hydroarylation

Zhu, Chuan,Song, Shengjin,Zhou, Lu,Wang, Ding-Xing,Feng, Chao,Loh, Teck-Peng

supporting information, p. 9482 - 9485 (2017/09/01)

An unprecedented Rh-catalyzed C2-difluoroalkylation of indole derivatives with 2,2-difluorovinyl arenesulfonates has been reported. This reaction provides a rare instance of catalytic difluoroalkylation through hydroarylation of gem-difluoroalkenes. The sulfonate group works as a chelating ligand, thus stabilizing the rhodacycle intermediate, leading to the uncommon transformation.

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