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

38858-90-1

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38858-90-1 Usage

Uses

4-Methyl-3-nitropyrazole is used in the synthesis of 4-(N-azolyl)-3,5-dinitropyrazoles.

Check Digit Verification of cas no

The CAS Registry Mumber 38858-90-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,8,5 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 38858-90:
(7*3)+(6*8)+(5*8)+(4*5)+(3*8)+(2*9)+(1*0)=171
171 % 10 = 1
So 38858-90-1 is a valid CAS Registry Number.
InChI:InChI=1S/C4H5N3O2/c1-3-2-5-6-4(3)7(8)9/h2H,1H3,(H,5,6)

38858-90-1SDS

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 4-Methyl-3-nitropyrazole

1.2 Other means of identification

Product number -
Other names 4-Methyl-5-nitro-1H-pyrazole

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:38858-90-1 SDS

38858-90-1Relevant academic research and scientific papers

INHIBITORS OF NECROPTOSIS

-

Page/Page column 73, (2021/09/04)

This invention relates to compounds of Formula (I) and salts, solvates, prodrugs, tautomers, N-oxides, stereoisomers, polymorphs and physiologically functional derivatives thereof. Also disclosed are methods of use of Formula (I), including in the inhibition of necroptosis and treatment of associated diseases, conditions and/or disorders.

HETEROCYCLE SUBSTITUTED AMINO-PYRIDINE COMPOUNDS AND METHODS OF USE THEREOF

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Paragraph 0435; 0437, (2016/04/20)

The present disclosure relates to heterocycle substituted amino-pyridine compounds. The present disclosure also relates to pharmaceutical compositions containing these compounds and methods of treating cancer by administering these compounds and pharmaceutical compositions to subjects in need thereof. The present disclosure also relates to the use of such compounds for research or other non-therapeutic purposes.

Faujasite catalyzed nitrodeiodination of iodopyrazoles

Ravi,Tewari, Surya P.

, p. 35 - 39 (2013/09/12)

Nitrodeiodination of iodopyrazoles using nitric acid/Faujasite has been investigated. The present procedure is simple, rapid and convenient and requires no sulfuric acid or oleum and may be applied for the synthesis of several nitropyrazoles in good yield

A simple and environmentally benign nitration of pyrazoles by impregnated bismuth nitrate

Ravi,Gore, Girish M.,Tewari, Surya P.,Sikder, Arun K.

, p. 1322 - 1327 (2014/01/06)

We report herein a facile, rapid, and environmentally friendly synthesis of nitropyrazoles in good yields using silica-bismuth nitrate and silica-sulfuric acid-bismuth nitrate at room temperature for the first time. The relatively non-toxic nature, ease o

Silica-sulfuric acid catalyzed nitrodeiodination of iodopyrazoles

Ravi,Gore, Girish M.,Sikder, Arun K.,Tewari, Surya P.

experimental part, p. 3463 - 3471 (2012/09/22)

We report here the synthesis of nitropyrazoles in good to excellent yields from iodopyrazoles over silica-sulfuric acid catalyst for the first time. The present procedure require less acid, offers a simplified workup procedure, and may be applied for the

Facile and environmentally friendly synthesis of nitropyrazoles using montmorillonite K-10 impregnated with bismuth nitrate

Ravi,Tewari, Surya P.

experimental part, p. 37 - 41 (2012/04/10)

Nitropyrazoles in higher yields were synthesized using montmorillonite K-10 impregnated with bismuth nitrate and the present procedure may be applied for the nitration of a wide variety of azoles in the drug and pharmaceutical industries.

Nitropyrazoles 17.* Synthesis of 1-(3,5-dinitrophenyl)-4-methyl-3,5- dinitropyrazole and the study of its chemical transformations

Zaitsev,Zaiko,Dalinger,Kachala,Shkineva,Shevelev

scheme or table, p. 2122 - 2128 (2011/01/11)

A new one-step method for the synthesis of 4-methyl-3(5)-nitropyrazole by nitration of 4-methylpyrazole is developed. Arylation of 4-methyl-3(5)- nitropyrazole with 1,3,5-trinitrobenzene gives 1-(3,5-dinitrophenyl)-4-methyl-3- nitropyrazole, nitration of

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