1-(2-Hydroxyethyl)cyclopropanol

Base Information

• Chemical Name: 1-(2-Hydroxyethyl)cyclopropanol
• CAS No.: 128312-78-7
• Molecular Formula: C5H10O2
• Molecular Weight: 102.133
• European Community (EC) Number: 869-445-3
• Mol file: 128312-78-7.mol

Synonyms:1-(2-hydroxyethyl)cyclopropanol;1-(2-hydroxyethyl)cyclopropan-1-ol;128312-78-7;SCHEMBL373949;RNVXPSVEYCEKOX-UHFFFAOYSA-N;MFCD22056252;AKOS027251207;SB16116;AS-32950;CS-0052907;EN300-5250347;A857344

Chemical Property of 1-(2-Hydroxyethyl)cyclopropanol

Chemical Property:

• Boiling Point: 240.5±8.0 °C(Predicted)
• PKA: 14.90±0.20(Predicted)
• PSA: 40.46000
• Density: 1.219±0.06 g/cm3(Predicted)
• LogP: -0.10630
• XLogP3: 0.1
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 102.068079557
• Heavy Atom Count: 7
• Complexity: 66.5

Purity/Quality:

97% ^*data from raw suppliers

1-(2-Hydroxyethyl)cyclopropanol 95+% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: C1CC1(CCO)O

Technology Process of 1-(2-Hydroxyethyl)cyclopropanol

There total 1 articles about 1-(2-Hydroxyethyl)cyclopropanol 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: 85.3%

1-[2-(tetrahydro-2H-pyran-2-yloxy)ethyl]-cyclopropanol (1221443-25-9) → 1-(2-hydroxyethyl)cyclopropanol (128312-78-7)

Guidance literature:

With pyridinium p-toluenesulfonate; In methanol; at 40 ℃;

Reference yield: 46.0%

1-(2-hydroxyethyl)cyclopropanol (128312-78-7) + p-toluenesulfonyl chloride (98-59-9) → 2-(1-hydroxycyclopropyl)ethyl 4-methylbenzene-1-sulfonate (128312-81-2)

Guidance literature:

With triethylamine; In dichloromethane; at 0 - 20 ℃; for 5h; Inert atmosphere;

Reference yield:

1-(2-hydroxyethyl)cyclopropanol (128312-78-7) + (3S)-ethyl 3-(4-((3-(4-hydroxy-2-methylphenyl)benzo[b]thiophen-5-yl)methoxy)phenyl)hex-4-ynoate → (3S)-ethyl 3-(4-((3-(4-(2-(1-hydroxycyclopropyl)ethoxy)-2-methylphenyl)benzo[b]thiophen-5-yl)methoxy)phenyl)hex-4-ynoate

Guidance literature:

With triphenylphosphine; 1,1'-azodicarbonyl-dipiperidine; In tetrahydrofuran; Inert atmosphere;

upstream raw materials:

1-[2-(tetrahydro-2H-pyran-2-yloxy)ethyl]-cyclopropanol

Downstream raw materials:

2-(1-hydroxycyclopropyl)ethyl 4-methylbenzene-1-sulfonate

N-(3-fluoro-4-(7-(2-(1-hydroxycyclopropyl)ethoxy)quinolin-4-yloxy)phenyl)-1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamide

1-(2-(4-(4-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamido)-2-fluorophenoxy)quinolin-7-yloxy)ethyl)cyclopropyl 2-(tert-butoxycarbonylamino)acetate

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