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946-65-6

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946-65-6 Usage

General Description

3-(Trifluoromethylthio)benzoic acid has trifluoromethylthio group. This group is useful for the preparation of new dyes, medicinal agents and novel heterocyclic systems.

Check Digit Verification of cas no

The CAS Registry Mumber 946-65-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,4 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 946-65:
(5*9)+(4*4)+(3*6)+(2*6)+(1*5)=96
96 % 10 = 6
So 946-65-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H5F3O2S/c9-8(10,11)14-6-3-1-2-5(4-6)7(12)13/h1-4H,(H,12,13)/p-1

946-65-6 Well-known Company Product Price

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  • Alfa Aesar

  • (A19975)  3-(Trifluoromethylthio)benzoic acid, 97%   

  • 946-65-6

  • 1g

  • 866.0CNY

  • Detail
  • Alfa Aesar

  • (A19975)  3-(Trifluoromethylthio)benzoic acid, 97%   

  • 946-65-6

  • 5g

  • 2988.0CNY

  • Detail

946-65-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(Trifluoromethylthio)benzoic acid

1.2 Other means of identification

Product number -
Other names 3-(trifluoromethylsulfanyl)benzoic acid

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:946-65-6 SDS

946-65-6Relevant articles and documents

Electrochemical Trifluoromethylation of Thiophenols with Sodium Trifluoromethanesulfinate

Zhu, Xing-Xing,Wang, Huai-Qin,Li, Chen-Guang,Xu, Xiao-Lan,Xu, Jun,Dai, Jian-Jun,Xu, Hua-Jian

, p. 16114 - 16120 (2021/02/03)

We developed an electrochemical trifluoromethylation of thiophenols without the use of metal catalysts and oxidants. This reaction features mild reaction conditions, readily available substrate, as well as moderate to good yields. In addition, this protocol can be easily scaled up with moderate efficiency.

Sandmeyer trifluoromethylthiolation of arenediazonium salts with sodium thiocyanate and Ruppert-Prakash reagent

Danoun, Gregory,Bayarmagnai, Bilguun,Gruenberg, Matthias F.,Goossen, Lukas J.

, p. 1312 - 1316 (2014/03/21)

In the presence of copper thiocyanate, sodium thiocyanate and the inexpensive, easy-to-use trifluoromethylating reagent Me3Si-CF 3, diazonium salts are smoothly converted into the corresponding aryl trifluoromethyl thioethers. Combin

ACID-BASE PROPERTIES OF (PERFLUOROALKYLTHIO)- AND (PERFLUOROALKYLSULFONYL)-SUBSTITUTED BENZOIC ACIDS AND ANILINES

Kondratenko, N. V.,Kolomeitsev, A. A.,Popov, V. I.,Il'chenko, A. Ya.,Korzhenevskaya, N. G.,et al.

, p. 2254 - 2258 (2007/10/02)

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