1,1,1-trifluorononan-2-one

Base Information Edit

Chemical Name:1,1,1-trifluorononan-2-one
CAS No.:26902-66-9
Molecular Formula:C9H15 F3 O
Molecular Weight:196.21
Hs Code.:
Mol file:26902-66-9.mol

Synonyms:1,1,1-Trifluorononan-2-one;Heptyl trifluoromethyl ketone; Trifluoromethyl heptyl ketone

Suppliers and Price of 1,1,1-trifluorononan-2-one

Supply Marketing:Edit

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

Total 3 raw suppliers

Chemical Property of 1,1,1-trifluorononan-2-one Edit

Chemical Property:

Vapor Pressure:1.02mmHg at 25°C
Boiling Point:177.8°C at 760 mmHg
Flash Point:90.1°C
Density:1.029g/cm³

Purity/Quality:: 99%, ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Use Description 1,1,1-Trifluorononan-2-one, a chemical compound, has several applications across different fields. In the field of organic chemistry, it is utilized as a valuable synthetic building block, serving as a starting material for the creation of more complex fluorinated compounds. This is crucial for drug development, as fluorinated molecules often exhibit enhanced pharmacological properties. In the realm of materials science, 1,1,1-trifluorononan-2-one can be employed in the production of specialty polymers and coatings, benefiting industries such as aerospace and electronics, where its unique properties contribute to improved performance and durability. Additionally, it plays a role in research and development, serving as a precursor for the synthesis of novel compounds in academia and industry, facilitating advancements in chemistry and materials science. Its versatility as a fluorinated compound makes it indispensable in these fields, driving innovation and progress in various applications.

Technology Process of 1,1,1-trifluorononan-2-one

There total 15 articles about 1,1,1-trifluorononan-2-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: 92.0%

: 122977-63-3
trifluoro-1,1,1 trimethylsilyloxy-2 nonene-2

: 26902-66-9
1,1,1-trifluorononan-2-one

Guidance literature:: With hydrogen fluoride; In dichloromethane; for 2h; Ambient temperature;
DOI:10.1016/S0022-1139(00)82782-7

Reference yield: 57.0%

: 124-07-2
Octanoic acid

: 383-63-1
ethyl trifluoroacetate,

: 26902-66-9
1,1,1-trifluorononan-2-one

Guidance literature:: Octanoic acid; With n-butyllithium; diisopropylamine; In tetrahydrofuran; hexane; at -65 - 20 ℃; for 2h; Inert atmosphere;

ethyl trifluoroacetate,; at -65 - 20 ℃; for 1h;
DOI:10.1002/anie.202104031