1-fluoro-2-methylpropane

Base Information

Chemical Name:1-fluoro-2-methylpropane
CAS No.:359-00-2
Molecular Formula:C4H9F
Molecular Weight:76.1139
Hs Code.:2903399090
DSSTox Substance ID:DTXSID901028436
Nikkaji Number:J395F
Wikidata:Q12880832
Mol file:359-00-2.mol

Synonyms:1-fluoro-2-methyl-propane;sec-butylfluoride;Isobutylfluoride;α-Fluor-isobutan;1-Fluor-2-methyl-propan;2-methylpropyl fluoride;

Suppliers and Price of 1-fluoro-2-methylpropane

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

Total 6 raw suppliers

Chemical Property of 1-fluoro-2-methylpropane

Chemical Property:

Vapor Pressure:757mmHg at 25°C
Melting Point:-110.8°C (estimate)
Refractive Index:1.3200
Boiling Point:15.47°C (estimate)
PSA：0.00000
Density:0.7500
LogP:1.61190
XLogP3:1.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:76.068828449
Heavy Atom Count:5
Complexity:17.6

Purity/Quality:: 98%min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)CF

Technology Process of 1-fluoro-2-methylpropane

There total 3 articles about 1-fluoro-2-methylpropane 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:

: 16156-53-9
isobutyl methanesulfonate

: 359-00-2
1-fluoro-2-methylpropane

: 2088-35-9
1,1-dichlorocyclopropane

Guidance literature:: isobutyl methanesulfonate; With potassium fluoride; In diethylene glycol; at 95 ℃; for 7.5h; Inert atmosphere;

With chloroform; N-benzyl-N,N,N-triethylammonium chloride; potassium hydroxide; In water; at 0 - 20 ℃; for 8.5h; Reagent/catalyst;