Methyl 2,3-dichloro-3-phenylpropanoate

Base Information

Chemical Name:Methyl 2,3-dichloro-3-phenylpropanoate
CAS No.:35115-84-5
Molecular Formula:C₁₀H₁₀Cl₂O₂
Molecular Weight:233.094
Hs Code.:
NSC Number:168956
DSSTox Substance ID:DTXSID70305074
Nikkaji Number:J1.150.386A

Synonyms:35115-84-5;methyl 2,3-dichloro-3-phenylpropanoate;NSC168956;SCHEMBL8925930;DTXSID70305074;NSC-168956

Suppliers and Price of Methyl 2,3-dichloro-3-phenylpropanoate

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

Total 4 raw suppliers

Chemical Property of Methyl 2,3-dichloro-3-phenylpropanoate

Chemical Property:

Vapor Pressure:0.00102mmHg at 25°C
Boiling Point:301.9°Cat760mmHg
Flash Point:122.8°C
Density:1.276g/cm³
XLogP3:2.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:232.0057849
Heavy Atom Count:14
Complexity:191

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC(=O)C(C(C1=CC=CC=C1)Cl)Cl

Technology Process of Methyl 2,3-dichloro-3-phenylpropanoate

There total 23 articles about Methyl 2,3-dichloro-3-phenylpropanoate 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: 90.0%

: 103-26-4,1754-62-7
methyl cinnamate

: 16492-74-3,17091-39-3,35115-84-5,49601-86-7,49601-88-9,118759-86-7,118759-87-8
methyl erythro-2,3-dichloro-3-phenylpropanoate

Guidance literature:: With sulfuryl dichloride; Triphenylphosphine oxide; In chloroform; at 20 ℃; for 1h; diastereoselective reaction;
DOI:10.1039/c6ra20101f

Reference yield: 70.0%

: 103-26-4,1754-62-7
Methyl cinnamate

: 16492-74-3,17091-39-3,35115-84-5,49601-86-7,49601-88-9,118759-86-7,118759-87-8
methyl erythro-2,3-dichloro-3-phenylpropanoate

Guidance literature:: With hydrogenchloride; dihydrogen peroxide; In tetrachloromethane; at 20 ℃;
DOI:10.1016/S0040-4020(99)00628-6

Reference yield: 51.0%

: 694-59-7
pyridine N-oxide

: 103-26-4,1754-62-7
Methyl cinnamate

: 16492-74-3,17091-39-3,35115-84-5,49601-86-7,49601-88-9,118759-86-7,118759-87-8
erythro-2,3-dichloro-3-phenylpropionic acid methyl ester

: threo-2,3-dichloro-3-phenylpropionic acid methyl ester

: erythro-N-(2-Chloro-2-methoxycarbonyl-1-phenylethoxy)pyridinium iodide

: threo-N-(2-Chloro-2-methoxycarbonyl-1-phenylethoxy)pyridinium iodide

Guidance literature:: pyridine N-oxide; Methyl cinnamate; With chlorine; In chloroform; at 20 - 25 ℃;

With potassium iodide; In chloroform;