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926247-77-0

926247-77-0

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926247-77-0 Usage

Appearance

White to light yellow solid

Purity

97%

Use

Building block in pharmaceutical and agrochemical industries for the synthesis of drugs and pesticides

Functional groups

Trifluoromethoxy and thiobenzamide

Value

Valuable intermediate in organic synthesis

Purity importance

High purity makes it a reliable and sought-after reagent for chemical research and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 926247-77-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,6,2,4 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 926247-77:
(8*9)+(7*2)+(6*6)+(5*2)+(4*4)+(3*7)+(2*7)+(1*7)=190
190 % 10 = 0
So 926247-77-0 is a valid CAS Registry Number.

926247-77-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail

  • Alfa Aesar

  • (H33047)  2-(Trifluoromethoxy)thiobenzamide, 97%   

  • 926247-77-0

  • 1g

  • 771.0CNY

  • Detail

  • Alfa Aesar

  • (H33047)  2-(Trifluoromethoxy)thiobenzamide, 97%   

  • 926247-77-0

  • 5g

  • 2570.0CNY

  • Detail

926247-77-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(Trifluoromethoxy)benzenecarbothioamide

1.2 Other means of identification

Product number -
Other names -

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:926247-77-0 SDS

926247-77-0Downstream Products

926247-77-0Relevant articles and documents

A efficient protocol for the synthesis of thioamides in [DBUH][OAc] at room temperature

Cao, Xian-Ting,Qiao, Li,Zheng, Hui,Yang, Hui-Yong,Zhang, Peng-Fei

, p. 170 - 175 (2018)

A novel, simple and eco-friendly method to synthesize thioamides from aryl nitriles and sodium sulfide (Na2S·9H2O) catalyzed by 1,8-diazabicyclo[5,4,0]undec-7-enium acetate ([DBUH][OAc]) ionic liquid (IL) at room temperature was developed in this paper. In this reaction, readily available inorganic salt (Na2S·9H2O) serves as the sulfur source, and various functional groups of aryl nitriles were well tolerated at room temperature. In addition, the products were easily separated from the IL which could be reused at least five times without considerable loss of its activity and applied in the green, concise synthesis of ethionamide.

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