2-Hexynoic acid, pentafluorophenyl ester

Base Information

Chemical Name:2-Hexynoic acid, pentafluorophenyl ester
CAS No.:201009-31-6
Molecular Formula:C12H7F5O2
Molecular Weight:278.178
Hs Code.:
DSSTox Substance ID:DTXSID80473253
Wikidata:Q82302546

Synonyms:2-Hexynoic acid, pentafluorophenyl ester;201009-31-6;DTXSID80473253

Suppliers and Price of 2-Hexynoic acid, pentafluorophenyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 2-Hexynoic acid, pentafluorophenyl ester

Chemical Property:

XLogP3:4.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:3
Exact Mass:278.03662027
Heavy Atom Count:19
Complexity:372

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCC#CC(=O)OC1=C(C(=C(C(=C1F)F)F)F)F

Technology Process of 2-Hexynoic acid, pentafluorophenyl ester

There total 1 articles about 2-Hexynoic acid, pentafluorophenyl ester 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:

: 764-33-0
hex-2-ynoic acid

: 771-61-9
2,3,4,5,6-pentafluorophenol

: 201009-31-6
Hex-2-ynoic acid pentafluorophenyl ester

Guidance literature:: With dmap; dicyclohexyl-carbodiimide; In dichloromethane; at -20 - 20 ℃;
DOI:10.1039/a704927g DOI:10.1016/S0040-4020(97)10385-4

Reference yield:

: 201009-31-6
Hex-2-ynoic acid pentafluorophenyl ester

: 17102-64-6
Sorbyl alcohol

Guidance literature:: With diisobutylaluminium hydride; triphenylphosphine; Yield given. Multistep reaction; 1) toluene, 50 deg C, 5 h; 2) toluene, 0 deg C, 30 min;
DOI:10.1016/S0040-4020(97)10385-4