Welcome to LookChem.com Sign In|Join Free

CAS

  • or

129922-51-6

Post Buying Request

129922-51-6 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

129922-51-6 Usage

General Description

1,1'-biphenyl, 2-[(trifluoromethyl)thio]- is a chemical compound that is composed of two benzene rings connected by a single carbon-carbon bond. It is also known as 2-(trifluoromethylthio)biphenyl. 1,1'-BIPHENYL, 2-[(TRIFLUOROMETHYL)THIO]- is commonly used as a building block in the synthesis of various organic compounds and can be found in a wide range of industrial applications. It is known to have properties that make it useful in the production of specialty chemicals, pharmaceuticals, and other materials. Additionally, it is important to handle this chemical with care due to its potential hazards and risks to human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 129922-51-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,9,2 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 129922-51:
(8*1)+(7*2)+(6*9)+(5*9)+(4*2)+(3*2)+(2*5)+(1*1)=146
146 % 10 = 6
So 129922-51-6 is a valid CAS Registry Number.

129922-51-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenyl-2-(trifluoromethylsulfanyl)benzene

1.2 Other means of identification

Product number -
Other names 2-[(Trifluoromethyl)thio]biphenyl

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:129922-51-6 SDS

129922-51-6Relevant articles and documents

Metal-Free Direct Trifluoromethylthiolation of Aromatic Compounds Using Triptycenyl Sulfide Catalyst

Kurose, Ryo,Nishii, Yuji,Miura, Masahiro

supporting information, p. 2380 - 2385 (2021/04/05)

Herein we report an efficient synthetic method for the electrophilic trifluoromethylthiolation of aromatic compounds. The key is to use triptycenyl sulfide (Trip-SMe) and TfOH to enhance the electrophilicity of SCF3 fragment through the formation of sulfonium intermediates. This method enables direct installation of an SCF3 group onto unactivated aromatics at room temperature, adopting a commercially available saccharin-based reagent. Preliminary DFT calculation was carried out to investigate the substitution effect on the catalytic activity.

Pd-catalyzed synthesis of Ar-SCF3 compounds under mild conditions

Teverovskiy, Georgiy,Surry, David S.,Buchwald, Stephen L.

supporting information; experimental part, p. 7312 - 7314 (2011/10/03)

Good to excellent yields of aryl trifluoromethyl sulfides, which are an important class of compounds in both the pharmaceutical and agrochemical areas, can be achieved under mild conditions by the Pd-catalyzed reaction of aryl bromides with a trifluoromethylthiolate nucleophile (see scheme). Copyright

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 129922-51-6