5-Methyl-2(5H)-furanone

Base Information

Chemical Name:5-Methyl-2(5H)-furanone
CAS No.:591-11-7
Molecular Formula:C5H6 O2
Molecular Weight:98.1014
Hs Code.:
European Community (EC) Number:209-700-2
NSC Number:11835,655
UNII:1AX0NCS144
DSSTox Substance ID:DTXSID901014526
Nikkaji Number:J13.667K
Wikidata:Q27116831
ChEMBL ID:CHEMBL47969
Mol file:591-11-7.mol

Synonyms:alpha-angelicalactone;angelica lactone;angelica lactone, (alpha)-isomer;angelica lactone, (beta)-isomer

Suppliers and Price of 5-Methyl-2(5H)-furanone

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

TRC
5-?Methylfuran-?2(5H)?-?one
50mg
$ 145.00

Chemenu
5-methylfuran-2(5H)-one 95%
1g
$ 393.00

Alichem
5-Methylfuran-2(5H)-one
250mg
$ 179.76

Total 19 raw suppliers

Chemical Property of 5-Methyl-2(5H)-furanone

Chemical Property:

Vapor Pressure:0.197mmHg at 25°C
Melting Point:<-17 °C
Refractive Index:1.4454
Boiling Point:210°C at 760 mmHg
Flash Point:78.9°C
PSA：26.30000
Density:1.095g/cm³
LogP:0.48790
Storage Temp.:2-8°C
XLogP3:0.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:98.036779430
Heavy Atom Count:7
Complexity:115

Purity/Quality:

97% ^*data from raw suppliers

5-?Methylfuran-?2(5H)?-?one ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1C=CC(=O)O1
Uses 5-?Methylfuran-?2(5H)?-?one can be used in analytical study of improved molecular level identification of organic compounds using comprehensive two-?dimensional chromatography, dual ionization energies and high resolution mass spectrometry.

Technology Process of 5-Methyl-2(5H)-furanone

There total 70 articles about 5-Methyl-2(5H)-furanone 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: 95.0%

: 201230-82-2
carbon monoxide

: 74785-04-9
(2R*,3Z)-4-Iodo-3-buten-2-ol

: 591-11-7
5-methyl-5H-furan-2-one

Guidance literature:: With potassium carbonate; hydrazine; bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; at 35 ℃; for 72h; under 2280 Torr;
DOI:10.1021/ja00532a034

Reference yield: 93.0%

: 1617-32-9
(E)-3-pentenoic acid

: 591-11-7
5-methyl-5H-furan-2-one

Guidance literature:: (E)-3-pentenoic acid; With Oxalyl bromide; dimethyl sulfoxide; In dichloromethane; at -10 - 20 ℃; for 1.16667h; Inert atmosphere;

With potassium carbonate; In dichloromethane-d2; water; at 20 ℃; for 5h; Inert atmosphere;

Reference yield: 93.0%

: 5204-64-8
3-pentenoic acid

: 591-11-7
5-methyl-5H-furan-2-one

Guidance literature:: 3-pentenoic acid; With Oxalyl bromide; dimethyl sulfoxide; In dichloromethane; at -10 - 20 ℃; Inert atmosphere;

With sodium hydroxide; In dichloromethane; water; for 5h; Reagent/catalyst;
DOI:10.1080/00397911.2019.1652914