72411-50-8

Basic information

• Product Name: 2-(4-BROMO-PHENYL)-5-PHENYL-2H-PYRAZOL-3-YLAMINE
• Synonyms: 2-(4-BROMO-PHENYL)-5-PHENYL-2H-PYRAZOL-3-YLAMINE;1-(4-BROMOPHENYL)-3-PHENYL-1H-PYRAZOL-5-AMINE;SALOR-INT L318396-1EA;5-Amino-1-(4-bromophenyl)-3-phenyl-1H-pyrazole;5-Amino-1-(4-bromophenyl)-3-phenyl-1H-pyrazole 97%;2-(4-bromophenyl)-5-phenylpyrazol-3-amine
• CAS NO: 72411-50-8
• Molecular Formula: C₁₅H₁₂BrN₃
• Molecular Weight: 314.18
• Mol File: 72411-50-8.mol

Chemical Properties

• Melting Point: 164-168 °C
• Boiling Point: 489.6±40.0 °C(Predicted)
• Appearance: /
• Density: 1.47±0.1 g/cm3(Predicted)
• PKA: 2.50±0.10(Predicted)
• CAS DataBase Reference: 2-(4-BROMO-PHENYL)-5-PHENYL-2H-PYRAZOL-3-YLAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-BROMO-PHENYL)-5-PHENYL-2H-PYRAZOL-3-YLAMINE(72411-50-8)
• EPA Substance Registry System: 2-(4-BROMO-PHENYL)-5-PHENYL-2H-PYRAZOL-3-YLAMINE(72411-50-8)

Safety Data

• Hazard Codes: Xi
• Statements: 41
• Safety Statements: 26-39
• WGK Germany: 3
• Hazardous Substances Data: 72411-50-8(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
2-(4-BROMO-PHENYL)-5-PHENYL-2H-PYRAZOL-3-YLAMINE is used as a potential pharmaceutical agent for its unique molecular structure and properties. It may contribute to the development of new drugs or drug candidates due to its chemical reactivity and the possibility of forming various derivatives.
Used in Agricultural Industry:
In agriculture, 2-(4-BROMO-PHENYL)-5-PHENYL-2H-PYRAZOL-3-YLAMINE may be utilized as a chemical intermediate for the synthesis of agrochemicals, such as pesticides or herbicides, given its potential reactivity and structural features.
Used in Material Science:
2-(4-BROMO-PHENYL)-5-PHENYL-2H-PYRAZOL-3-YLAMINE could be employed in material science for the development of new materials with specific properties, such as high thermal stability or unique electronic characteristics, owing to its chemical composition and structure.
Further research is necessary to fully explore and understand the potential uses and effects of 2-(4-BROMO-PHENYL)-5-PHENYL-2H-PYRAZOL-3-YLAMINE in these and other industries.

Upstream product

• 614-16-4 Benzoylacetonitrile 
• 589-21-9 (4-bromophenyl)hydrazine 

Downstream Products

• 1400634-64-1 1-(4-bromophenyl)-3-phenyl-1H-pyrazolo[3,4-d]pyrimidine 
• 1602492-81-8 (E)-1,2-bis(1-(4-bromophenyl)-3-phenyl-1H-pyrazol-5-yl)diazene 
• 1602492-71-6 (E)-1,2-bis(1-(4-bromophenyl)-4-iodo-3-phenyl-1H-pyrazol-5-yl)diazene 
• 1439359-38-2 C₂₉H₂₂BrN₃O₃ 
• 1354574-64-3 1'-(4-bromophenyl)-1',4'-dihydro-3'-phenylspiro[acenaphthylene-1(2H),11'-[11H]benzo[g]pyrazolo[4,3-b]quinoline]-2,5',10'-trione 
• 1354574-58-5 1-(4-bromophenyl)-1,4-dihydro-3-phenylspiro[11H-benzo-[g]pyrazolo[4,3-b]quinoline-11,3'-[3H]indole]-2',5,10(1'H)-trione 
• 1354574-61-0 1-(4-bromophenyl)-1,4-dihydro-3-phenyl-1'-(phenylmethyl)spiro[11H-benzo[g]pyrazolo-[4,3-b]quinoline-11,3'-[3H]indole]-2',5,10(1'H)-trione 
• 1315269-04-5 1-(4-bromophenyl)-3-phenyl-1H-spiro[indeno[1,2-b]pyrazolo[4,3-e]pyridine-4,3'-indoline]-2',5(10H)-dione 
• 1315269-13-6 1-(4-bromophenyl)-5'-nitro-3-phenyl-1H-spiro[indeno[1,2-b]pyrazolo[4,3-e]pyridine-4,3'-indoline]-2',5(10H)-dione 
• 1315269-09-0 5'-bromo-1-(4-bromophenyl)-3-phenyl-1H-spiro[indeno[1,2-b]pyrazolo[4,3-e]pyridine-4,3'-indoline]-2',5(10H)-dione 
• 1315269-17-0 1-(4-bromophenyl)-1'-methyl-3-phenyl-1H-spiro[indeno[1,2-b]pyrazolo[4,3-e] pyridine-4,3'-indoline]-2',5(10H)-dione 
• 1310545-74-4 5'-bromo-1-(4-bromophenyl)-1'-ethyl-1,11-dihydro-3-phenylspiro[benzo[g]pyrazolo[3,4-b]quinoline-4,3'-indole]-2',5,10(1'H)-trione 
• 1310545-83-5 C₃₇H₂₀BrN₃O₃ 
• 1310545-70-0 C₃₃H₁₉BrN₄O₃ 

Relevant articles and documents

Visible-light enabled C4-thiocyanation of pyrazoles by graphite-phase carbon nitride (g-C3N4)

Thiocyanation is an important and effective way to form C[sbnd]S bonds in organic synthetic methodology. Especially, thiocyanation of pyrazole attracts the attention of many researchers because sulfur-containing compounds are widely applied in many crucial fields such as organic materials, agrochemistry, nanotechnology, etc. Herein, we described A rapid metal- and additive-free method for C(sp2)-H thiocyanation of pyrazoles under visible light at room temperature by using a sustainable catalyst of graphite-phase carbon nitride (g-C3N4) and a thiocyanating agent of ammonium thiocyanate. The method presents many advantages, such as usage of eco-friendly photoredox catalyst, a wide range of substrates and a good yield of products, etc.