2-Chloropentan-3-one

Base Information

Chemical Name:2-Chloropentan-3-one
CAS No.:17042-21-6
Molecular Formula:C5H9 Cl O
Molecular Weight:120.579
Hs Code.:2914700090
DSSTox Substance ID:DTXSID80455276
Nikkaji Number:J597.891B
Mol file:17042-21-6.mol

Synonyms:2-chloropentan-3-one;17042-21-6;3-Pentanone, 2-chloro-;2-Chloro-3-pentanone;2-Chlorpentanon-3 Wasser;SCHEMBL5492354;DTXSID80455276;AKOS010226417;1,1-BIPHENYL,4-METHYL-4-NITRO-;EN300-119398

Suppliers and Price of 2-Chloropentan-3-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

TRC
2-chloropentan-3-one
250mg
$ 265.00

American Custom Chemicals Corporation
2-CHLOROPENTAN-3-ONE 95.00%
5MG
$ 498.85

AK Scientific
2-Chloropentan-3-one
10g
$ 1586.00

AK Scientific
2-Chloropentan-3-one
100mg
$ 189.00

Total 8 raw suppliers

Chemical Property of 2-Chloropentan-3-one

Chemical Property:

PSA：17.07000
LogP:1.59280
XLogP3:1.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:120.0341926
Heavy Atom Count:7
Complexity:70.5

Purity/Quality:

98%min ^*data from raw suppliers

2-chloropentan-3-one ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCC(=O)C(C)Cl
General Description 2-Chloropentan-3-one (also known as 2-Chloro-3-pentanone) is an α-chloro ketone that serves as a key intermediate in organic synthesis, particularly in the preparation of chiral compounds such as (S)-(+)-manicone, an alarm pheromone of Manica ants. It can be converted into functionalized ketimines for further alkylation and stereoselective transformations, demonstrating its utility in the synthesis of enantiopure natural products.

Technology Process of 2-Chloropentan-3-one

There total 15 articles about 2-Chloropentan-3-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: 80.0%