Phenoxyacetone

Base Information

Chemical Name:Phenoxyacetone
CAS No.:621-87-4
Molecular Formula:C9H10O2
Molecular Weight:150.177
Hs Code.:29145000
European Community (EC) Number:210-712-5
NSC Number:1876
UNII:ZKT38MGG38
DSSTox Substance ID:DTXSID3060740
Nikkaji Number:J1.674H
Wikidata:Q63399121
Mol file:621-87-4.mol

Synonyms:phenoxyacetone

Suppliers and Price of Phenoxyacetone

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
Phenoxy-2-propanone
1g
$ 65.00

TCI Chemical
Phenoxyacetone >97.0%(GC)
25g
$ 432.00

TCI Chemical
Phenoxyacetone >97.0%(GC)
5g
$ 124.00

Sigma-Aldrich
Phenoxy-2-propanone 97%
5g
$ 30.90

Matrix Scientific
1-Phenoxy-propan-2-one 95%+
10g
$ 900.00

Matrix Scientific
1-Phenoxy-propan-2-one 95%+
5g
$ 486.00

Matrix Scientific
1-Phenoxy-propan-2-one 95%+
1g
$ 108.00

Crysdot
1-Phenoxypropan-2-one 95+%
5g
$ 124.00

Crysdot
1-Phenoxypropan-2-one 95+%
10g
$ 208.00

Crysdot
1-Phenoxypropan-2-one 95+%
25g
$ 332.00

Total 39 raw suppliers

Chemical Property of Phenoxyacetone

Chemical Property:

Appearance/Colour:Clear light yellow liquid
Vapor Pressure:0.0666mmHg at 25°C
Refractive Index:n20/D 1.521(lit.)
Boiling Point:230.2 °C at 760 mmHg
Flash Point:85 °C
PSA：26.30000
Density:1.045 g/cm³
LogP:1.65440
Storage Temp.:2-8°C
Solubility.:Chloroform (Slightly), Ethyl Acetate (Slightly)
XLogP3:1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:150.068079557
Heavy Atom Count:11
Complexity:126

Purity/Quality:

98% ^*data from raw suppliers

Phenoxy-2-propanone ^*data from reagent suppliers

Safty Information:

Pictogram(s): T
Hazard Codes:T
Statements: 23
Safety Statements: 45

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)COC1=CC=CC=C1
Uses Phenoxy-2-propanone is a general chemical reagent used in the preparation of α-arylthio ketones via DL-proline. Phenoxy-2-propanone was used in the preparation of 3-mercapto-5-methyl-1-phenoxy-methyl-4-phenyl-1,2,4-triazolinium hydroxide inner salt.

Technology Process of Phenoxyacetone

There total 43 articles about Phenoxyacetone 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: 99.9%

: 78-95-5
chloroacetone

: 108-95-2,27073-41-2
phenol

: 621-87-4
3-phenoxy-2-propanone

Guidance literature:: phenol; With potassium carbonate; In acetone; at 20 ℃; for 0.5h;

chloroacetone; With potassium iodide; In acetone; for 3h; Reflux;

Reference yield: 98.0%

: 1451053-96-5
5-phenoxymethyl-1,2,3-oxadiazole 3-oxide

: 621-87-4
3-phenoxy-2-propanone

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In methanol; at 20 ℃; for 2h; under 760.051 Torr;
DOI:10.3987/COM-12-S(N)127