2,3-Diphenylpropanol

Base Information

• Chemical Name: 2,3-Diphenylpropanol
• CAS No.: 3536-29-6
• Molecular Formula: C15H16 O
• Molecular Weight: 212.291
• Hs Code.: 2906299090
• European Community (EC) Number: 222-572-2
• DSSTox Substance ID: DTXSID80871033
• Nikkaji Number: J144.990G
• Mol file: 3536-29-6.mol

Synonyms:2,3-Diphenylpropanol;3536-29-6;EINECS 222-572-2;2,3-Diphenyl-1-propanol;1-Propanol, 2,3-diphenyl-;SCHEMBL597894;DTXSID80871033;AKOS015157985

Chemical Property of 2,3-Diphenylpropanol

Chemical Property:

• Vapor Pressure: 6.41E-05mmHg at 25°C
• Melting Point: 51°C
• Refractive Index: 1.5742 (estimate)
• Boiling Point: 331°Cat760mmHg
• Flash Point: 134.4°C
• PSA: 20.23000
• Density: 1.073g/cm³
• LogP: 3.00520
• XLogP3: 3.2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 4
• Exact Mass: 212.120115130
• Heavy Atom Count: 16
• Complexity: 178

Purity/Quality:

98%Min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)CC(CO)C2=CC=CC=C2

Technology Process of 2,3-Diphenylpropanol

There total 51 articles about 2,3-Diphenylpropanol 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: 99.0%

2,3-diphenylpropanoic acid (94942-89-9) → 2,3-diphenyl-1-propanol (3536-29-6)

Guidance literature:

With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 - 20 ℃; Inert atmosphere;

DOI:10.1002/ejoc.202100355

Reference yield: 98.0%

(E)-2,3-diphenyl-propenal (13702-35-7,1755-47-1) → 2,3-diphenyl-1-propanol (3536-29-6)

Guidance literature:

With palladium on activated charcoal; hydrogen; In methanol; under 760.051 Torr;

DOI:10.1039/c4ob02282c

Reference yield: 96.0%

2-phenylethanol (60-12-8) + benzyl alcohol (100-51-6,185532-71-2) → (1E)-1,3-diphenylpropene (3412-44-0) + 2,3-diphenyl-1-propanol (3536-29-6)

Guidance literature:

With potassium hydroxide; In toluene; at 110 ℃; for 96h;

DOI:10.1039/c2cc33101b

upstream raw materials:

potassium benzyloxide

phenylacetaldehyde

benzyl alcohol

2-phenylethanol

Downstream raw materials:

1,3-diphenylpropene

2,3-diphenyl-1-propene

1-bromo-2,3-diphenyl-propane

β-benzyl-phenethyl alcohol, p-toluenesulfonate