ETHYL MANDELATE

Base Information

Chemical Name:ETHYL MANDELATE
CAS No.:4358-88-7
Molecular Formula:C10H12O3
Molecular Weight:180.20000
Hs Code.:29172090
Mol file:4358-88-7.mol

Synonyms:DL-Mandelic Acid Ethyl Ester;Hydroxy-phenyl-acetic acid ethyl ester;Benzeneacetic acid, α-hydroxy-, ethyl ester, (±)-;Ethyl DL-Mandelate;

Suppliers and Price of ETHYL MANDELATE

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

Usbiological
Ethyl Mandelate
5g
$ 319.00

Sigma-Aldrich
Ethyl mandelate for synthesis
100 mL
$ 72.52

Total 45 raw suppliers

Chemical Property of ETHYL MANDELATE

Chemical Property:

Vapor Pressure:0.00918mmHg at 25°C
Melting Point:35.5°C
Refractive Index:n20/D 1.512(lit.)
Boiling Point:253-255oC(lit.)
Flash Point:>230 °F
PSA：46.53000
Density:1.115 g/mL at 25oC(lit.)
LogP:1.28310
Storage Temp.:Refrigerator
Solubility.:Chloroform (Slightly), Ethyl Acetate (Slightly)

Purity/Quality:

99% ^*data from raw suppliers

Ethyl Mandelate ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Safety Statements: 24/25

MSDS Files:: SDS file from LookChem

Useful:

Uses Ethyl Mandelate is used as a reagent in the synthesis of several organic compounds including that of volatile methylsiloxanes which have the potential to be a more environmentally sustainable alternative as solvents in chemical synthesis to non-polar organic solvents. It was found to act as a substrate for (S)-mandelate dehydrogenase which is a flavin mononucleotide dependent enzyme that oxidises (S)-mandelate to benzoylformate.

Technology Process of ETHYL MANDELATE

There total 75 articles about ETHYL MANDELATE 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: 100.0%

: 1603-79-8
phenylglyoxylic acid ethyl ester

: 774-40-3,4358-88-7
hydroxy-phenyl-acetic acid ethyl ester

Guidance literature:: With NADH model substance; magnesium(II); In acetonitrile; Ambient temperature;

Reference yield: 100.0%

: 64-17-5
ethanol

: 611-71-2,611-72-3,17199-29-0,90-64-2
MANDELIC ACID

: 774-40-3,4358-88-7
hydroxy-phenyl-acetic acid ethyl ester

Guidance literature:: With sulfuric acid; for 1.5h; Reflux;
DOI:10.1007/s00044-011-9805-z

Reference yield: 99.0%

: 924-44-7
glyoxylic acid ethyl ester

: 98-80-6
phenylboronic acid

: 774-40-3,4358-88-7
hydroxy-phenyl-acetic acid ethyl ester

Guidance literature:: With [Rh(OH)(cod)]2; (4aR,9aR)-6,8-dibenzyl-2,3-dimethoxy-2,3-dimethyl-3,4a,5,8,9,9a-hexahydro-2H-[1,4]dioxino[2,3-e][1,3]diazepin-6-ium hexafluorophosphate; potassium tert-butylate; In tert-Amyl alcohol; toluene; at 20 ℃; for 4h; Inert atmosphere;
DOI:10.1016/j.tet.2012.05.129