56367-24-9

Basic information

• Product Name: 5-ISOPROPYL-1H-PYRAZOL-3-AMINE
• Synonyms: 3-Isopropyl-1H-pyrazol-5-ylaMine;1H-Pyrazol-3-aMine, 5-(1-Methylethyl)-;EOS-60939
• CAS NO: 56367-24-9
• Molecular Formula: C₆H₁₁N₃
• Molecular Weight: 125.17
• Mol File: 56367-24-9.mol
• Article Data: 16

Chemical Properties

• Boiling Point: 299.7°C at 760 mmHg
• Flash Point: 160.3°C
• Appearance: /
• Density: 1.104g/cm³
• Vapor Pressure: 0.00117mmHg at 25°C
• Refractive Index: 1.57
• PKA: 15.60±0.10(Predicted)
• CAS DataBase Reference: 5-ISOPROPYL-1H-PYRAZOL-3-AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-ISOPROPYL-1H-PYRAZOL-3-AMINE(56367-24-9)
• EPA Substance Registry System: 5-ISOPROPYL-1H-PYRAZOL-3-AMINE(56367-24-9)

Safety Data

• Hazardous Substances Data: 56367-24-9(Hazardous Substances Data)

Usage

Uses

3-Isopropyl-1H-pyrazol-5-amine

InChI:InChI=1/C6H11N3/c1-4(2)5-3-6(7)9-8-5/h3-4H,1-2H3,(H3,7,8,9)

Upstream product

• 29509-06-6 4-methyl-3-oxopentanonitrile 
• 2861-04-3 4-methyl-2,3-pentadienenitrile 

Downstream Products

• 1616085-93-8 2-chloro-N-(5-isopropyl-1H-pyrazol-3-yl)-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-amine 
• 1403758-06-4 1-(4-((5-isopropyl-1H-pyrazol-3-yl)amino)phenyl)butan-1-one 
• 1258423-74-3 C₂₄H₃₁N₉OS 

Relevant articles and documents

Identification of TRD-35 as Potent and Selective DRAK2 Inhibitor

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Application of 5-aminopyrazole compounds to plant growth regulation aspect

The invention discloses application of 5-aminopyrazole compounds to plant growth regulation aspect in the technical field of pesticide compounds, in particular to application of the 5-aminopyrazole compounds shown by the formula to the plant growth regulation aspect, particularly the application to the plant growth inhibition. The formula I is shown in the description. The compound shown in the formula I can be used as a weedicide; weeds in places such as highway and railway can be killed through regulating the concentration of the 5-aminopyrazole compounds, wherein the R1 is hydrogen or alkylor phenyl or substituted phenyl; R2 is alkyl; R3 is hydrogen or halogen.

Direct synthesis of pyrazoles from esters using tert-butoxide-assisted C-(C=O) coupling

This paper describes the direct synthesis of pyrazoles from esters that comprises two sequential reactions: tert-butoxide-assisted C-C(=O) coupling reaction to yield β-ketonitrile or α,β-alkynone intermediates, and condensation by hydrazine addition. The method reported allows for easy control of the regioselectivity and structure of substituents at N-1, C-3, C-4 and/or C-5 positions.