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169213-73-4

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169213-73-4 Usage

General Description

(3-(trifluoroMethyl)-1H-pyrazol-5-yl)Methanol is a chemical compound with the molecular formula C7H7F3N2O. It is a derivative of pyrazole and contains a trifluoromethyl group. (3-(trifluoroMethyl)-1H-pyrazol-5-yl)Methanol has potential applications in the pharmaceutical industry, specifically as a building block for the synthesis of various bioactive molecules. It may also have uses in agrochemicals or materials science. The presence of the trifluoromethyl group makes this compound an important target for synthetic chemists and researchers interested in developing new functional materials. Additional research and testing may be necessary to fully understand the potential properties and applications of (3-(trifluoroMethyl)-1H-pyrazol-5-yl)Methanol.

Check Digit Verification of cas no

The CAS Registry Mumber 169213-73-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,2,1 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 169213-73:
(8*1)+(7*6)+(6*9)+(5*2)+(4*1)+(3*3)+(2*7)+(1*3)=144
144 % 10 = 4
So 169213-73-4 is a valid CAS Registry Number.

169213-73-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-(trifluoromethyl)-1H-pyrazol-5-yl]methanol

1.2 Other means of identification

Product number -
Other names [3-(trifluoromethyl)pyrazol-5-yl]methan-1-ol

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:169213-73-4 SDS

169213-73-4Downstream Products

169213-73-4Relevant articles and documents

Synthesis of 3-perfluoroalkyl-, including 3-trifluoromethyl-, substituted pyrazoles from perfluoroalkylacetylenes

Tang, Xiao-Qing,Hu, Chang-Ming

, p. 129 - 132 (1995)

3-Perfluoroalkylpyrazoles 2 have been prepared in excellent yield by the reactions of perfluoroalkylacetylenes 1 with hydrazine monohydrate under mild conditions. - Keywords: Perfluoroalkylpyrazoles; Synthesis; Perfluoroalkylacetylenes; Hydrazene; Nucleop

PYRAZOLEALKANAMIDE SUBSTITUTED THIOPHENES AS AMPA POTENTIATORS

-

Page/Page column 58-59, (2008/06/13)

The present invention relates to a heterocyclic derivative according to Formula (I) wherein the variables are defined as in the specification, or to a pharmaceutically acceptable salt or solvate thereof. The present invention also relates to a pharmaceuti

A novel and practical method for the synthesis of 3-trifluoromethylated pyrazoles

Tang,Hu

, p. 631 - 632 (2007/10/02)

A new building block strategy for the synthesis of a series of 3-trifluoromethyl substituted pyrazoles 4 by a two-step sequence is described.

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