Benzyl alcohol, alpha-vinyl-, carbamate

Base Information

• Chemical Name: Benzyl alcohol, alpha-vinyl-, carbamate
• CAS No.: 73826-14-9
• Molecular Formula: C10H11NO2
• Molecular Weight: 177.1998
• DSSTox Substance ID: DTXSID90994924
• Nikkaji Number: J87.379I
• Mol file: 73826-14-9.mol

Synonyms:73826-14-9;Benzyl alcohol, alpha-vinyl-, carbamate;BRN 3251666;2-Propen-1-ol, 1-phenyl-, carbamate;Phenyl-vinyl-carbinol-carbamat [German];Phenyl-vinyl-carbinol-carbamat;Benzenemethanol, alpha-ethenyl-, carbamate;Carbamic acid 1-phenyl-2-propen-1-yl ester;1-PHENYL-2-PROPEN-1-OL CARBAMATE;SCHEMBL3828726;DTXSID90994924;LS-123791;Benzenemethanol, .alpha.-ethenyl-, carbamate;1-Phenylprop-2-en-1-yl hydrogen carbonimidate

Chemical Property of Benzyl alcohol, alpha-vinyl-, carbamate

Chemical Property:

• Vapor Pressure: 0.000201mmHg at 25°C
• Boiling Point: 327.5°Cat760mmHg
• Flash Point: 167.6°C
• PSA: 52.32000
• Density: 1.119g/cm³
• LogP: 2.70930
• XLogP3: 2.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 177.078978594
• Heavy Atom Count: 13
• Complexity: 185

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C=CC(C1=CC=CC=C1)OC(=O)N

Technology Process of Benzyl alcohol, alpha-vinyl-, carbamate

There total 1 articles about Benzyl alcohol, alpha-vinyl-, carbamate 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:

Carbamidsaeure-(1-phenyl-propin-(2)-ylester) (3567-38-2) → carbamic acid 1-phenylallyl ester (73826-14-9)

Guidance literature:

With methanol; Lindlar's catalyst; Hydrogenation;

Reference yield: 60.0%

carbamic acid 1-phenylallyl ester (73826-14-9) → carbamic acid 3-phenylallyl ester (1078-70-2)

Guidance literature:

With palladium diacetate; lithium chloride; In tetrahydrofuran; at 40 ℃;

DOI:10.1055/s-0028-1083282

upstream raw materials:

Carbamidsaeure-(1-phenyl-propin-(2)-ylester)

Downstream raw materials:

carbamic acid 3-phenylallyl ester

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