2-(1,2-Dihydroxyethyl)-5-ethoxytetrahydrofuran-3,4-diol

Base Information Edit

Chemical Name:2-(1,2-Dihydroxyethyl)-5-ethoxytetrahydrofuran-3,4-diol
CAS No.:13403-13-9
Molecular Formula:C8H16 O6
Molecular Weight:208.211
Hs Code.:
NSC Number:170174
DSSTox Substance ID:DTXSID30305313
Mol file:13403-13-9.mol

Synonyms:NSC170174;686298-98-6;2-(1,2-Dihydroxyethyl)-5-ethoxytetrahydrofuran-3,4-diol;13403-13-9;DTXSID30305313;NSC-170174

Suppliers and Price of 2-(1,2-Dihydroxyethyl)-5-ethoxytetrahydrofuran-3,4-diol

Supply Marketing:Edit

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 2 raw suppliers

Chemical Property of 2-(1,2-Dihydroxyethyl)-5-ethoxytetrahydrofuran-3,4-diol Edit

Chemical Property:

Vapor Pressure:8.56E-10mmHg at 25°C
Boiling Point:445.1°Cat760mmHg
Flash Point:223°C
Density:1.4g/cm³
XLogP3:-1.7
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:4
Exact Mass:208.09468823
Heavy Atom Count:14
Complexity:175

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC1C(C(C(O1)C(CO)O)O)O

Technology Process of 2-(1,2-Dihydroxyethyl)-5-ethoxytetrahydrofuran-3,4-diol

There total 10 articles about 2-(1,2-Dihydroxyethyl)-5-ethoxytetrahydrofuran-3,4-diol 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: 81.0%

: 64-17-5
ethanol

: 100645-45-2
(4-nitro)phenyl β-D-galactofuranoside

: 13403-13-9
ethyl-β-D-galactofuranoside

Guidance literature:: With α-L-arabinofuranosidase from ruminiclostridium thermocellum L29V mutant; In aq. phosphate buffer; at 25 ℃; for 3h; pH=7; Reagent/catalyst; Kinetics; Enzymatic reaction;
DOI:10.1039/c9ob01162e

Reference yield:

: 59-23-4
D-Galactose

: 13403-13-9
ethyl-β-D-galactofuranoside

Guidance literature:: Multi-step reaction with 2 steps

1: aqueous hydrochloric acid

2: mercury (II)-chloride; mercury (II)-oxide

With hydrogenchloride; mercury dichloride; mercury(II) oxide;
DOI:10.1021/ja01286a015