13788-94-8

Basic information

• Product Name: 1H-Pyrazole,3,5-dimethyl-1-(4-nitrophenyl)-
• Synonyms: 1H-Pyrazole,3,5-dimethyl-1-(4-nitrophenyl)-;3,5-dimethyl-1-(4-nitrophenyl)pyrazole
• CAS NO: 13788-94-8
• Molecular Formula: C₁₁H₁₁N₃O₂
• Molecular Weight: 217.2239
• Mol File: 13788-94-8.mol
• Article Data: 22

Chemical Properties

• Boiling Point: 356.7°C at 760 mmHg
• Flash Point: 169.5°C
• Appearance: /
• Density: 1.26g/cm³
• Vapor Pressure: 5.9E-05mmHg at 25°C
• Refractive Index: 1.621
• CAS DataBase Reference: 1H-Pyrazole,3,5-dimethyl-1-(4-nitrophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrazole,3,5-dimethyl-1-(4-nitrophenyl)-(13788-94-8)
• EPA Substance Registry System: 1H-Pyrazole,3,5-dimethyl-1-(4-nitrophenyl)-(13788-94-8)

Safety Data

• Hazardous Substances Data: 13788-94-8(Hazardous Substances Data)

Usage

Structure

Pyrazole derivative with two methyl groups at the 3 and 5 positions, and a 4-nitrophenyl group at the 1 position

Usage

Commonly used in organic synthesis and pharmaceutical research

Biological activities

Exhibits various biological activities, including anti-inflammatory and anticancer properties

Building block

Used as a building block in the synthesis of various heterocyclic compounds

Potential applications

Has potential applications in the development of new drugs and agrochemicals due to its diverse pharmacological and biological properties.

InChI:InChI=1/C11H11N3O2/c1-8-7-9(2)13(12-8)10-3-5-11(6-4-10)14(15)16/h3-7H,1-2H3

Upstream product

• 1131-16-4 3,5-dimethyl-1-phenyl-1H-pyrazole 
• 861801-83-4 4,4-bis-[N'-(4-nitro-phenyl)-hydrazino]-pentan-2-one 
• 64-19-7 acetic acid 
• 100-16-3 4-nitrophenylhydrazone 
• 123-54-6 acetylacetone 
• 636-99-7 4-nitrophenylhydrazine hydrochloride 
• 7732-18-5 water 
• 67-51-6 3,5-dimethyl-1H-pyrazole 
• 100-25-4 para-dinitrobenzene 
• 586-78-7 para-nitrophenyl bromide 
• 410522-20-2 3-acetyl-1-phenyl-1-methyl-4-(methylamino)-3-penten-2-one 
• 162129-85-3 3-acetyl-1,1-diphenyl-4-(methylamino)-3-penten-2-one 
• 410522-21-3 3-acetyl-1,1-dimethyl-4-(methylamino)-3-penten-2-one 
• 1118-66-7 4-Aminopent-3-en-2-one 

Downstream Products

• 99845-58-6 3,5-dimethyl-4-nitro-1-p-nitrophenylpyrazole 
• 130967-93-0 N-[(Z)-1-{2-[3,5-Dimethyl-1-(4-nitro-phenyl)-1H-pyrazole-4-carbonyl]-phenylcarbamoyl}-2-(4-methoxy-phenyl)-vinyl]-benzamide 
• 52708-32-4 3,5-dimethyl-1-(4'-aminophenyl)-1H-pyrazole 
• 1215212-17-1 C₁₁H₁₀FN₃O₂ 
• 1215212-18-2 4-fluoro-3-fluoromethyl-5-methyl-1-(4-nitrophenyl)pyrazole 
• 123271-94-3 1-[4-(3,5-Dimethyl-pyrazol-1-yl)-phenyl]-3-(2-hydroxy-4,4-dimethyl-6-oxo-cyclohex-1-enyl)-2,6,6-trimethyl-1,5,6,7-tetrahydro-indol-4-one 
• 13808-93-0 4-bromo-3,5-dimethyl-1-p-nitrophenylpyrazole 

Relevant articles and documents

Tunable aryl alkyl ionic liquids (TAAILs) based on 1-aryl-3,5-dimethyl-1H-pyrazoles

A series of fifteeen new 1-aryl-2,3,5-trimethylpyrazolium salts ([PhRC1pz][X], R: 4-Cl, 4-Br, 4-Me, 4-OMe, 4-NO2; C1: methyl, X: methanesulfonate [CH3SO3?], tetrafluoroborate [BF

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Novel 1-phenyl-1H-pyrazole derivatives and use thereof

The present invention provides a novel 1 -phenyl -1. H-The present invention relates to pyrazole derivatives and uses thereof. , The present invention 1 -phenyl -1 exhibits an excellent anti-proliferative effect on cancer cells. H-The present invention relates to a pyrazole derivative compound, a pharmaceutically acceptable salt thereof, a hydrate or stereoisomer thereof, a pharmaceutical composition for preventing, alleviating, or treating cancer metastasis and proliferative diseases comprising the same as an active ingredient.

HBF4/ACN: A simple and efficient protocol for the synthesis of pyrazoles under ambient reaction conditions

An efficient and novel protocol for pyrazole synthesis has been developed by using fluoroboric acid as the acid catalyst. Simple and easily available 1,3-diketone and hydrazine derivatives are taken as the substrates for this purpose. The reaction entails