1-(Fluoromethyl)-2-methylbenzene

Base Information

Chemical Name:1-(Fluoromethyl)-2-methylbenzene
CAS No.:62037-88-1
Molecular Formula:C8H9F
Molecular Weight:124.158
Hs Code.:
DSSTox Substance ID:DTXSID70577451
Nikkaji Number:J432.230D
Wikidata:Q82467474

Synonyms:1-(Fluoromethyl)-2-methylbenzene;62037-88-1;SCHEMBL864780;DTXSID70577451

Suppliers and Price of 1-(Fluoromethyl)-2-methylbenzene

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 0 raw suppliers

Chemical Property of 1-(Fluoromethyl)-2-methylbenzene

Chemical Property:

XLogP3:2.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:124.068828449
Heavy Atom Count:9
Complexity:80.6

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=CC=C1CF

Technology Process of 1-(Fluoromethyl)-2-methylbenzene

There total 6 articles about 1-(Fluoromethyl)-2-methylbenzene 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: 68.0%

: 62037-88-1
1-(fluoromethyl)-2-methylbenzene

Guidance literature:: With potassium fluoride; formic acid; tetramethylammonium fluoride; N,N`-sulfuryldiimidazole; In N,N-dimethyl-formamide; at 20 ℃; for 4h; Inert atmosphere;

Reference yield: 36.0%

: 95-47-6
o-xylene

: 452-64-2
3,4-dimethyl-fluorobenzene

: 62037-88-1
1-(fluoromethyl)-2-methylbenzene

: 443-82-3
3-fluoro-o-xylene

Guidance literature:: With caesium fluoroxysulphate; In acetonitrile; at 35 - 40 ℃; for 1h; Yields of byproduct given;
DOI:10.1021/jo00026a032