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3-Methyl-4-nitro-pyrazole-1-carboxylic acid tert-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

847139-22-4

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847139-22-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 847139-22-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,7,1,3 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 847139-22:
(8*8)+(7*4)+(6*7)+(5*1)+(4*3)+(3*9)+(2*2)+(1*2)=184
184 % 10 = 4
So 847139-22-4 is a valid CAS Registry Number.

847139-22-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 3-methyl-4-nitropyrazole-1-carboxylate

1.2 Other means of identification

Product number -
Other names tert-butyl 5-methyl-4-nitro-1H-pyrazole-1-carboxylate

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:847139-22-4 SDS

847139-22-4Relevant academic research and scientific papers

VEGFR3 INHIBITORS

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Page/Page column 129, (2014/03/22)

This invention relates to a compound of the formula (I): The invention also relates to processes for the preparation of the compound of the formula (I), pharmaceutical agents or compositions containing the compound or a method of using the compound for th

Chiral phosphoric acid-catalyzed enantioselective three- component aza-diels-alder reactions of aminopyrroles and aminopyrazoles

Brioche, Julien,Courant, Thibaut,Alcaraz, Lilian,Stocks, Michael,Furber, Mark,Zhu, Jieping,Masson, Geraldine

supporting information, p. 1719 - 1724 (2014/06/09)

A highly stereoselective three-component Povarov reaction, catalyzed by (R)- and (S)-BINOL hydrogen phosphate, was achieved for the first time with aminopyrroles and aminopyrazoles as 2-azadiene precursors. A variety of aldehydes, enecarbamates, amino-substituted azines participated in the reaction to afford the tetrahydropyrrolopyridines and tetrahydropyrazolopyridines in good yields with excellent diatereo- and enantioselectivities. A stereochemical model is proposed to account for the observed absolute stereochemistry.

PYRIDINE COMPOUNDS

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Page/Page column 205, (2010/01/12)

The present invention relates to compounds that inhibit of focal adhesion kinase function, processes for their preparation, pharmaceutical compositions containing them as the active ingredient, to their use as medicaments and to their use in the manufacture of medicaments for use in the treatment in warm-blooded animals such as humans of diseases such as cancer.

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