Egomaketone

Base Information

Chemical Name:Egomaketone
CAS No.:59204-74-9
Molecular Formula:C₁₀H₁₂O₂
Molecular Weight:164.204
Hs Code.:
UNII:O37E2Q1R62
DSSTox Substance ID:DTXSID90207945
Nikkaji Number:J11.166J
Wikidata:Q27285265
Metabolomics Workbench ID:48092
Mol file:59204-74-9.mol

Synonyms:EGOMAKETONE;Egomacetone;59204-74-9;1-(furan-3-yl)-4-methylpent-3-en-1-one;HSDB 3484;3-Penten-1-one, 1-(3-furanyl)-4-methyl-;UNII-O37E2Q1R62;3-(4-methyl-3-pentenoyl)furan;O37E2Q1R62;3-Penten-1-one;EGOMACETONE [HSDB];DTXSID90207945;CHEBI:180397;AKOS006277386;1-Furan-3-yl-4-methylpent-3-en-1-one;LS-63762;1-furan-3-yl-4-methyl-pent-3-en-1-one;1-(3-Furanyl)-4-methyl-3-Penten-1-one;1-(uran-3-yl)-4-methylpent-3-en-1-one;1-(3-Furanyl)-4-methyl-3-penten-1-one, 9CI;3-PENTEN-1-ONE, 1-(3-FURYL)-4-METHYL-;Q27285265

Suppliers and Price of Egomaketone

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

American Custom Chemicals Corporation
EGOMAKETONE 95.00%
5MG
$ 495.59

Total 5 raw suppliers

Chemical Property of Egomaketone

Chemical Property:

Vapor Pressure:0.03mmHg at 25°C
Boiling Point:244.6°C at 760 mmHg
Flash Point:106.5°C
PSA：30.21000
Density:1.006g/cm³
LogP:2.81860
XLogP3:2.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:164.083729621
Heavy Atom Count:12
Complexity:190

Purity/Quality:

97% ^*data from raw suppliers

EGOMAKETONE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Chemical Classes:Biological Agents -> Plant Oils and Extracts
Canonical SMILES:CC(=CCC(=O)C1=COC=C1)C

Technology Process of Egomaketone

There total 8 articles about Egomaketone 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: 80.0%

: 123030-45-5
1-furan-3-yl-4-methyl-pent-3-en-1-ol

: 59204-74-9
egomaketone

Guidance literature:: With pyridinium chlorochromate; In dichloromethane;
DOI:10.1021/jo00284a040

Reference yield: 80.0%

: 82187-40-4
1-Furan-3-yl-4-methyl-2-(2-methylamino-benzenesulfonyl)-pent-3-en-1-one

: 59204-74-9
egomaketone

Guidance literature:: With hydrogen; nickel;
DOI:10.1248/cpb.30.1106

Reference yield: 75.0%

: 201230-82-2
carbon monoxide

: 78952-50-8
3-(Trimethylstannyl)furan

: 503-60-6
3,3-dimethyl-allyl chloride

: 59204-74-9
egomaketone

Guidance literature:: With triphenylphosphine; bis(dibenzylideneacetone)-palladium⁽⁰⁾; In chloroform; at 25 ℃; for 24h; under 2327.2 - 2585.7 Torr;
DOI:10.1021/ja00329a032