Methyl [2-(4-bromophenyl)-1-hydroxy-2-oxoethyl]carbamate

Base Information

Chemical Name:Methyl [2-(4-bromophenyl)-1-hydroxy-2-oxoethyl]carbamate
CAS No.:88073-11-4
Molecular Formula:C₁₀H₁₀BrNO₄
Molecular Weight:288.098
Hs Code.:
DSSTox Substance ID:DTXSID40519409

Synonyms:88073-11-4;DTXSID40519409;Methyl [2-(4-bromophenyl)-1-hydroxy-2-oxoethyl]carbamate

Suppliers and Price of Methyl [2-(4-bromophenyl)-1-hydroxy-2-oxoethyl]carbamate

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
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Total 0 raw suppliers

Chemical Property of Methyl [2-(4-bromophenyl)-1-hydroxy-2-oxoethyl]carbamate

Chemical Property:

XLogP3:1.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:286.97932
Heavy Atom Count:16
Complexity:264

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC(=O)NC(C(=O)C1=CC=C(C=C1)Br)O

Technology Process of Methyl [2-(4-bromophenyl)-1-hydroxy-2-oxoethyl]carbamate

There total 3 articles about Methyl [2-(4-bromophenyl)-1-hydroxy-2-oxoethyl]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: 66.8%

: 88073-02-3
ethyl phenacyloxycarbamate

: 38192-19-7
methyl 2-phenyl-1-hydroxy-2-oxoethylcarbamate

: 41260-63-3
ethyl (2-phenyl-1-hydroxy-2-oxoethyl)carbamate

: 88073-11-4
methyl 2-p-bromophenyl-1-hydroxy-2-oxoethylcarbamate

: 88073-10-3
ethyl 2-p-bromophenyl-1-hydroxy-2-oxoethylcarbamate

Guidance literature:: With triethylamine; In benzene-d6; at 30 ℃; Rate constant; Mechanism; kinetic isotope effect; different reagents, solvent and reaction time;