3-Hydroxy-4-(2-hydroxyethyl)furan-2(5H)-one

Base Information

Chemical Name:3-Hydroxy-4-(2-hydroxyethyl)furan-2(5H)-one
CAS No.:114533-59-4
Molecular Formula:C6H8O4
Molecular Weight:144.127
Hs Code.:
DSSTox Substance ID:DTXSID40555948
Wikidata:Q82437405
Mol file:114533-59-4.mol

Synonyms:3-hydroxy-4-(2-hydroxy-ethyl)-5h-furan-2-one;114533-59-4;3-Hydroxy-4-(2-hydroxyethyl)furan-2(5H)-one;BPLVXTDBBDMMEY-UHFFFAOYSA-;DTXSID40555948;InChI=1/C6H8O4/c7-2-1-4-3-10-6(9)5(4)8/h7-8H,1-3H2

Suppliers and Price of 3-Hydroxy-4-(2-hydroxyethyl)furan-2(5H)-one

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 1 raw suppliers

Chemical Property of 3-Hydroxy-4-(2-hydroxyethyl)furan-2(5H)-one

Chemical Property:

XLogP3:-0.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:144.04225873
Heavy Atom Count:10
Complexity:182

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C(=C(C(=O)O1)O)CCO

Technology Process of 3-Hydroxy-4-(2-hydroxyethyl)furan-2(5H)-one

There total 1 articles about 3-Hydroxy-4-(2-hydroxyethyl)furan-2(5H)-one 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: 33.0%

: 141509-41-3
4-methylene-1-oxa-6,9-diazaspiro<4,5>decane-7,10-dione

: 1668-10-6
glycinamide hydrochloride

: 114533-59-4
3-hydroxy-4-(2-hydroxyethyl)-2(5H)-furanone

Guidance literature:: With hydrogenchloride; at 100 ℃; for 1.5h; Product distribution; other conditions, other reagents;
DOI:10.1021/jo00039a028