m-(2,3-Dihydroxypropoxy)benzoic acid methyl ester

Base Information

Chemical Name:m-(2,3-Dihydroxypropoxy)benzoic acid methyl ester
CAS No.:67032-33-1
Molecular Formula:C11H14O5
Molecular Weight:226.23
Hs Code.:
Mol file:67032-33-1.mol

Synonyms:m-(2,3-Dihydroxypropoxy)benzoic acid,methyl ester;BENZOIC ACID,m-(2,3-DIHYDROXYPROPOXY)-,METHYL ESTER;

Suppliers and Price of m-(2,3-Dihydroxypropoxy)benzoic acid methyl ester

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 3 raw suppliers

Chemical Property of m-(2,3-Dihydroxypropoxy)benzoic acid methyl ester

Chemical Property:

Vapor Pressure:1.92E-07mmHg at 25°C
Boiling Point:409.6°C at 760 mmHg
Flash Point:160.2°C
PSA：75.99000
Density:1.258g/cm³
LogP:0.20520

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of m-(2,3-Dihydroxypropoxy)benzoic acid methyl ester

There total 4 articles about m-(2,3-Dihydroxypropoxy)benzoic acid methyl ester 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: 97.0%

: 79250-46-7
methyl 3-(prop-2-enyloxy)benzoate

: 67032-33-1
methyl (±)-3-(2,3-dihydroxypropoxy)benzoate

Guidance literature:: With potassium osmate; 4-methylmorpholine N-oxide; In water; acetone; at 40 ℃; for 8h;
DOI:10.1002/ejoc.201901474

Reference yield:

: 99-06-9
3-Carboxyphenol

: 67032-33-1
methyl (±)-3-(2,3-dihydroxypropoxy)benzoate

Guidance literature:: Multi-step reaction with 3 steps

1: sulfuric acid / 7 h / Reflux

2: potassium carbonate; tetra-(n-butyl)ammonium iodide / acetone / 4 h / Reflux

3: potassium osmate; 4-methylmorpholine N-oxide / acetone; water / 8 h / 40 °C

With potassium osmate; sulfuric acid; tetra-(n-butyl)ammonium iodide; potassium carbonate; 4-methylmorpholine N-oxide; In water; acetone;
DOI:10.1002/ejoc.201901474

Reference yield:

: 19438-10-9
methyl 3-hydroxybenzoate

: 67032-33-1
methyl (±)-3-(2,3-dihydroxypropoxy)benzoate

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate; tetra-(n-butyl)ammonium iodide / acetone / 4 h / Reflux

2: potassium osmate; 4-methylmorpholine N-oxide / acetone; water / 8 h / 40 °C

With potassium osmate; tetra-(n-butyl)ammonium iodide; potassium carbonate; 4-methylmorpholine N-oxide; In water; acetone;
DOI:10.1002/ejoc.201901474