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20154-03-4

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20154-03-4 Usage

Chemical Properties

Colorless to light yellow liqui

Uses

Different sources of media describe the Uses of 20154-03-4 differently. You can refer to the following data:
1. 3-(Trifluoromethyl)pyrazole was determined to be a small compound inhibitor of human FATP2.
2. 3-(Trifluoromethyl)pyrazole may be used in copper-catalyzed pyrazole N-arylation. It may be used in the synthesis of sodium hydridotris(1H-3-trifluoromethylpyrazol-1-yl)borate by heating with sodium borohydride.

General Description

3-(Trifluoromethyl)pyrazoles is a heterocyclic building block. It undergoes alkylation with alkyl iodides in DMF to afford the N-alkyl pyrazoles. It participates in the synthesis of disubstituted pyrimidines.

Check Digit Verification of cas no

The CAS Registry Mumber 20154-03-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,1,5 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 20154-03:
(7*2)+(6*0)+(5*1)+(4*5)+(3*4)+(2*0)+(1*3)=54
54 % 10 = 4
So 20154-03-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H4ClF6N/c9-6-4(8(13,14)15)1-3(2-5(6)16)7(10,11)12/h1-2H,16H2

20154-03-4 Well-known Company Product Price

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  • Alfa Aesar

  • (H55068)  3-Trifluoromethyl-1H-pyrazole, 97%   

  • 20154-03-4

  • 250mg

  • 141.0CNY

  • Detail
  • Alfa Aesar

  • (H55068)  3-Trifluoromethyl-1H-pyrazole, 97%   

  • 20154-03-4

  • 1g

  • 394.0CNY

  • Detail
  • Alfa Aesar

  • (H55068)  3-Trifluoromethyl-1H-pyrazole, 97%   

  • 20154-03-4

  • 5g

  • 1191.0CNY

  • Detail
  • Aldrich

  • (406228)  3-(Trifluoromethyl)pyrazole  99%

  • 20154-03-4

  • 406228-1G

  • 558.09CNY

  • Detail
  • Aldrich

  • (406228)  3-(Trifluoromethyl)pyrazole  99%

  • 20154-03-4

  • 406228-5G

  • 1,664.91CNY

  • Detail

20154-03-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(Trifluoromethyl)pyrazole

1.2 Other means of identification

Product number -
Other names AKOS PAO-1199

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:20154-03-4 SDS

20154-03-4Upstream product

20154-03-4Relevant articles and documents

Gas-phase reactions of benzene and derivatives triggered by hydrazine/ozone; hydroxylation vs. degradation

Sol, Veronica M.,Mulder, Peter,Louw, Robert

, p. 577 - 582 (2007/10/02)

The reactions of benzene derivatives C6H5X (X = H, Cl, CH3 and CF3) with hydrazine and ozone in the dark (a source of OH radicals) have been studied in a flow reactor at ambient temperature. (Substituted) phenols were formed, but these were relatively unimportant compared to N-heterocyclic compounds (condensation products of cis-butenedial and analogues with hydrazine) and other (degradation) products.Benzene and (trifluoromethyl)benzene follow a similar path as toluene, also with oxidative ring opening as major reactions.

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