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25688-18-0

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25688-18-0 Usage

General Description

1-(3-nitrophenyl)-1H-pyrazole, also known as 3-nitrophenylpyrazole, is a chemical compound with the molecular formula C10H7N3O2. It is a yellow crystalline solid that is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is also utilized as a research reagent in organic synthesis and chemical analysis. 3-nitrophenylpyrazole has potential applications in the development of new drugs and insecticides due to its unique chemical structure and properties. However, it is important to handle this compound with caution as it may pose health and environmental hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 25688-18-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,6,8 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 25688-18:
(7*2)+(6*5)+(5*6)+(4*8)+(3*8)+(2*1)+(1*8)=140
140 % 10 = 0
So 25688-18-0 is a valid CAS Registry Number.

25688-18-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-nitrophenyl)pyrazole

1.2 Other means of identification

Product number -
Other names N-(3-nitrophenyl)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:25688-18-0 SDS

25688-18-0Relevant articles and documents

NURR1 RECEPTOR MODULATORS

-

Paragraph 0646; 1409-1411, (2020/09/08)

Described herein, inter alia, are Nurr1 receptor modulators and uses thereof. In an aspect is provided a method for treating a disease associated with dysregulation and/or degeneration of dopaminergic neurons in the central nervous system of a subject in need thereof, the method including administering to the subject in need thereof a therapeutically effective amount of a compound described herein.

N-Picolinamides as ligands for Ullmann-type C-N coupling reactions

Damkaci, Fehmi,Alawaed, Abdulkhaliq,Vik, Erik

supporting information, p. 2197 - 2200 (2016/05/02)

The use of N-phenyl-2-pyridincarboxamide-1-oxide as a ligand with Cu2O in Ullmann type C-N bond formations between aryl halides and N-heteroaryls in common solvents, such as MeCN, DMF, and DMSO at 82-120 °C has been successfully demonstrated. The ligand is effective when only 4% equiv is used relative to the substrate. The reaction provided the corresponding products in coupling of electron-rich, electron poor, and ortho-substituted aryl halides, including ortho aryl-chlorides, in good to very good yields. N-arylation is selectively preferred at the benzyl position when ortho-halide benzyl bromide is reacted with one equivalent of pyrazole. However, di-N-arylation is achieved in very high yields when 2.5 equiv of pyrazole is used, providing a stoichiometric control over the coupling reaction.

A 1,10-phenanthrene rowling-N-Monoxide derivatives ligand and its application

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Paragraph 0355-0366, (2016/11/21)

The invention relates to a 1,10-Phenanthroline monohydrate-dual N-monoxide derivative ligand. The derivative ligand has a structural formula as follows: FORMULA, wherein R1 and R8 are selected from hydrogen, halogen, hydroxyl, C1-C7 alkoxyl, straight-chain saturated or unsaturated C1-C6 alkyl, or branched-chain saturated or unsaturated C1-C6 alkyl; R2 to R7 are selected from hydrogen, halogen, hydroxyl, C1-C8 alkoxyl, straight-chain saturated or unsaturated C1-C6 alkyl, or branched-chain saturated or unsaturated C1-C6 alkyl, C3-C7 ring hydroxyl, benzyl, aryl or 5-7 membered heterocyclic ring. Hetero atoms (such as O or N) are contained in the ligand disclosed by the invention, and a transitional six-membered ring is formed through coordination with copper ions, so that aryl iodide, aryl bromide or aryl chloride is promoted to carry out a C-N coupling reaction with aliphatic amine or secondary aliphatic cyclammonium or aliphatic acid or nitrogen-containing heterocyclic compounds at room temperature.

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