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3-methoxy-1-methyl-4-nitropyrazole is a pyrazole derivative characterized by the presence of a nitro group, a methoxy group, and a methyl group at the 1-position on the pyrazole ring. This chemical compound has potential applications in the pharmaceutical industry and as a building block for the synthesis of various organic molecules, including energetic materials or explosives.

1201935-85-4

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1201935-85-4 Usage

Uses

Used in Pharmaceutical Industry:
3-methoxy-1-methyl-4-nitropyrazole is used as a building block for the development of new drugs and medications due to its unique structure and properties.
Used in Organic Synthesis:
3-methoxy-1-methyl-4-nitropyrazole is used as a valuable component in the synthesis of various organic molecules, leveraging its distinctive chemical structure.
Used in Energetic Materials or Explosives:
3-methoxy-1-methyl-4-nitropyrazole is used as a precursor in the synthesis of energetic materials or explosives, taking advantage of the presence of the nitro group in its structure.
Further research and exploration of the properties and potential applications of 3-methoxy-1-methyl-4-nitropyrazole are necessary to fully understand its utility and impact in different fields.

Check Digit Verification of cas no

The CAS Registry Mumber 1201935-85-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,1,9,3 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1201935-85:
(9*1)+(8*2)+(7*0)+(6*1)+(5*9)+(4*3)+(3*5)+(2*8)+(1*5)=124
124 % 10 = 4
So 1201935-85-4 is a valid CAS Registry Number.

1201935-85-4SDS

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 3-Methoxy-1-Methyl-4-Nitro-1H-Pyrazole

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:1201935-85-4 SDS

1201935-85-4Downstream Products

1201935-85-4Relevant academic research and scientific papers

C-H Amination of Nitro Azaheterocyclic Compounds by Vicarious Nucleophilic Substitution

Zhou, Ru-Shuang,Cai, Chun

supporting information, p. 88 - 92 (2021/12/03)

Various nitro azaheterocyclic compounds were subjected to C H amination by vicarious nucleophilic substitution with 4H-1,2,4-triazol-4-amine (ATA). The aminated products were characterized by NMR, mass spectroscopy, and single-crystal X-ray diffraction an

AROMATIC HETEROCYCLIC COMPOUND WITH KINASE INHIBITORY ACTIVITY

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Paragraph 0098-0100, (2021/07/29)

Provided are a JAK kinase inhibitor, preparation and use thereof. In particular, provided is a compound of Formula I, wherein each group is as described in the specification. The compound has an excellent JAK inhibitory activity, and therefore can be used to prepare pharmaceutical compositions for the treatment of cancer and other diseases related to JAK activity.

Alkynyl pyrimidine or alkynyl pyridine compound as well as composition and application thereof

-

Paragraph 0097; 0098; 0101, (2020/08/18)

The invention relates to alkynyl pyrimidine or alkynyl pyridine compounds represented by a formula (I) or pharmaceutically acceptable salts, isomers, solvates, crystals or prodrugs thereof. The invention also discloses a pharmaceutical composition contain

PYRIDINE COMPOUNDS

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Page/Page column 208, (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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