Benzyl vinylcarbamate

Base Information

Chemical Name:Benzyl vinylcarbamate
CAS No.:84713-20-2
Molecular Formula:C10H11NO2
Molecular Weight:177.203
Hs Code.:2924299090
European Community (EC) Number:840-814-0
DSSTox Substance ID:DTXSID60448747
Nikkaji Number:J428.598K
Wikidata:Q72443264
Mol file:84713-20-2.mol

Synonyms:benzyl N-vinylcarbamate;vinyl carbamate

Suppliers and Price of Benzyl vinylcarbamate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
BenzylVinylcarbamate
2.5g
$ 305.00

Crysdot
Benzylvinylcarbamate 95+%
1g
$ 248.00

Crysdot
Benzylvinylcarbamate 95+%
250mg
$ 99.00

Crysdot
Benzylvinylcarbamate 95+%
100mg
$ 62.00

Crysdot
Benzylvinylcarbamate 95+%
5g
$ 743.00

Biosynth Carbosynth
Benzyl Vinylcarbamate
2 g
$ 400.00

Biosynth Carbosynth
Benzyl Vinylcarbamate
1 g
$ 250.00

Biosynth Carbosynth
Benzyl Vinylcarbamate
250 mg
$ 100.00

Biosynth Carbosynth
Benzyl Vinylcarbamate
100 mg
$ 80.00

Biosynth Carbosynth
Benzyl Vinylcarbamate
500 mg
$ 160.00

Total 26 raw suppliers

Chemical Property of Benzyl vinylcarbamate

Chemical Property:

Vapor Pressure:0.006mmHg at 25°C
Melting Point:43-44°C
Refractive Index:1.529
Boiling Point:271.837 °C at 760 mmHg
PKA:11.04±0.46(Predicted)
Flash Point:118.203 °C
PSA：38.33000
Density:1.089 g/cm³
LogP:2.44720
Storage Temp.:Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
Solubility.:Chloroform (Slightly), Ethyl Acetate (Slightly)
XLogP3:2.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:177.078978594
Heavy Atom Count:13
Complexity:174

Purity/Quality:

97% ^*data from raw suppliers

BenzylVinylcarbamate ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Statements: 36/37/38
Safety Statements: 26-36/37/39

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C=CNC(=O)OCC1=CC=CC=C1
Uses Benzyl Vinylcarbamate is used as a reagent in the synthesis of CF3- or -?CF2-?substituted tetrahydroquinolines.

Technology Process of Benzyl vinylcarbamate

There total 10 articles about Benzyl vinylcarbamate 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: 78.0%

: 84713-20-2
benzyl N-vinylcarbamate

Guidance literature:: With 2,4,6-trimethyl-pyridine; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; palladium dichloride; CyJohnPhos; In N,N-dimethyl acetamide; at 20 ℃; for 15h; Schlenk technique; Inert atmosphere; Irradiation;