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1H-Pyrazole, 4-bromo-3,5-dimethyl-1-(triphenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

919802-98-5

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919802-98-5 Usage

Type of compound

pyrazole derivative

Bromine atom position

4th position

Methyl groups positions

3rd and 5th positions

Triphenylmethyl group position

1st position

Usage

organic synthesis and pharmaceutical research

Potential applications

building block for new compounds and drugs, development of pesticides, materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 919802-98-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,9,8,0 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 919802-98:
(8*9)+(7*1)+(6*9)+(5*8)+(4*0)+(3*2)+(2*9)+(1*8)=205
205 % 10 = 5
So 919802-98-5 is a valid CAS Registry Number.

919802-98-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-bromo-3,5-dimethyl-1-tritylpyrazole

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:919802-98-5 SDS

919802-98-5Relevant academic research and scientific papers

Efficient and chromatography-free methodology for the modular synthesis of oligo-(1H-pyrazol-4-yl)-arenes with controllable size, shape and steric bulk

Kershaw Cook, Laurence J.,Kearsey, Rachel,Lamb, Jessica V.,Pace, Edward J.,Gould, Jamie A.

supporting information, p. 895 - 898 (2016/02/05)

A novel methodology to synthesise oligo-(1H-pyrazol-4-yl)-arenes with controllable size, shape and steric bulk from 1-trityl-1H-pyrazol-4-ylboronate pinacol esters. This straightforward and efficient procedure can be applied to a variety of brominated aro

Mild and highly selective palladium-catalyzed monoarylation of ammonia enabled by the use of bulky biarylphosphine ligands and palladacycle precatalysts

Cheung, Chi Wai,Surry, David S.,Buchwald, Stephen L.

supporting information, p. 3734 - 3737 (2013/08/23)

A method for the Pd-catalyzed arylation of ammonia with a wide range of aryl and heteroaryl halides, including challenging five-membered heterocyclic substrates, is described. Excellent selectivity for monoarylation of ammonia to primary arylamines was achieved under mild conditions or at rt by the use of bulky biarylphosphine ligands (L6, L7, and L4) as well as their corresponding aminobiphenyl palladacycle precatalysts (3a, 3b, and 3c). As this process requires neither the use of a glovebox nor high pressures of ammonia, it should be widely applicable.

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