2-(1H-pyrazol-1-yl)propan-1-ol

Base Information

• Chemical Name: 2-(1H-pyrazol-1-yl)propan-1-ol
• CAS No.: 191725-73-2
• Molecular Formula: C₆H₁₀N₂O
• Molecular Weight: 126.158
• Hs Code.: 2933199090
• Mol file: 191725-73-2.mol

Synonyms:2-(1H-pyrazol-1-yl)propan-1-ol;02(3-Pyrazol-1-yl-phenyl)-methanol;Albb-004087;2-(1H-pyrazol-1-yl)-1-propanol(SALTDATA: FREE);2-(1H-Pyrazol-1-yl)-1-propanol

Chemical Property of 2-(1H-pyrazol-1-yl)propan-1-ol

Chemical Property:

• Vapor Pressure: 0.0499mmHg at 25°C
• Boiling Point: 225.2°C at 760 mmHg
• Flash Point: 90°C
• PSA: 38.05000
• Density: 1.12g/cm³
• LogP: 0.43640

Purity/Quality:

98%min ^*data from raw suppliers

2-(1H-pyrazol-1-yl)propan-1-ol ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 2-(1H-pyrazol-1-yl)propan-1-ol

There total 2 articles about 2-(1H-pyrazol-1-yl)propan-1-ol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 45.0%

ethyl 2-(1H-pyrazol-1-yl)propionate → 2-pyrazol-1-ylpropan-1-ol (191725-73-2)

Guidance literature:

With lithium aluminium tetrahydride; In tetrahydrofuran; diethyl ether; at 0 ℃; for 1h;

Reference yield:

NH-pyrazole (288-13-1) + methyloxirane (75-56-9,16033-71-9) → 2-pyrazol-1-ylpropan-1-ol (191725-73-2) + 1-pyrazol-1-yl-propan-2-ol

Guidance literature:

Y(NO₃)3*6H₂O; for 24h;

DOI:10.1016/j.tetlet.2008.03.152

upstream raw materials:

NH-pyrazole

methyloxirane

Refernces

• 1、 Bhanushali, Mayur J.,Nandurkar, Nitin S.,Bhor, Malhari D.,Bhanage, Bhalchandra M.. "Y(NO3)3·6H2O catalyzed regioselective ring opening of epoxides with aliphatic, aromatic, and heteroaromatic amines". . p. 3672 - 3676. Retrieved 2008/09/19.