Methylamine, N-heptafluorobutyryl-

Base Information

Chemical Name:Methylamine, N-heptafluorobutyryl-
CAS No.:4314-42-5
Molecular Formula:C5H4F7NO
Molecular Weight:227.082
Hs Code.:2924199090
DSSTox Substance ID:DTXSID20895591
Wikidata:Q82871855
Mol file:4314-42-5.mol

Synonyms:Methylamine, N-heptafluorobutyryl-;2,2,3,3,4,4,4-heptafluoro-n-methylbutanamide;4314-42-5;SCHEMBL11805773;N-methyl-heptafluorobutyric amide;DTXSID20895591;NS00109695;Butanamide, 2,2,3,3,4,4,4-heptafluoro-N-methyl-;Butyramide, 2,2,3,3,4,4,4-heptafluoro-N-methyl-

Suppliers and Price of Methylamine, N-heptafluorobutyryl-

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
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price

Total 1 raw suppliers

Chemical Property of Methylamine, N-heptafluorobutyryl-

Chemical Property:

PSA：29.10000
LogP:1.95620
XLogP3:2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:2
Exact Mass:227.01811089
Heavy Atom Count:14
Complexity:233

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CNC(=O)C(C(C(F)(F)F)(F)F)(F)F

Technology Process of Methylamine, N-heptafluorobutyryl-

There total 1 articles about Methylamine, N-heptafluorobutyryl- 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:

: 115584-92-4
(E)-2-Chloro-4,4,5,5,6,6,6-heptafluoro-3-hydroxy-hex-2-enoic acid methyl ester

: 96-30-0
chloroacetylmethylamide

: 4314-42-5
N-methyl-heptafluorobutyrylamide

: 113341-48-3
(Z)-4,4,5,5,6,6,6-Heptafluoro-3-hydroxy-hex-2-enoic acid methyl ester

Guidance literature:: In diethyl ether; at -40 ℃; for 1h;
DOI:10.1007/BF01557519

Reference yield:

: 4314-42-5
N-methyl-heptafluorobutyrylamide

: Benzoic acid (7R,8R,9S,13S,14S,17S)-17-acetoxy-7-{10-[(2,2,3,3,4,4,4-heptafluoro-butyl)-methyl-carbamoyl]-decyl}-13-methyl-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthren-3-yl ester

Guidance literature:: Multi-step reaction with 2 steps

1: borane-dimethyl-sulfide / tetrahydrofuran / Heating

2: 1) N-methylmorpholine, isobutyl chloroformate / 1) CH₂Cl₂, -10 deg C, 2) CH₂Cl₂, r.t.

With 4-methyl-morpholine; dimethylsulfide borane complex; isobutyl chloroformate; In tetrahydrofuran;
DOI:10.1016/0039-128X(89)90076-7