N-trifluoroacetyl-L-phenylalanine acid chloride

Base Information

Chemical Name:N-trifluoroacetyl-L-phenylalanine acid chloride
CAS No.:2252-71-3
Molecular Formula:C₁₁H₉ClF₃NO₂
Molecular Weight:279.646
Hs Code.:

Synonyms:N-trifluoroacetyl-L-phenylalanine acid chloride

Suppliers and Price of N-trifluoroacetyl-L-phenylalanine acid chloride

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 N-trifluoroacetyl-L-phenylalanine acid chloride

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N-trifluoroacetyl-L-phenylalanine acid chloride

There total 3 articles about N-trifluoroacetyl-L-phenylalanine acid chloride 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:

: 350-09-4
N-trifluoroacetyl-L-phenylalanine

: 2252-71-3
N-trifluoroacetyl-L-phenylalanine acid chloride

Guidance literature:: With thionyl chloride; benzene;
DOI:10.1021/ja01615a032

Reference yield:

: 63-91-2,25191-15-5,658-69-5,67675-33-6
L-phenylalanine

: 2252-71-3
N-trifluoroacetyl-L-phenylalanine acid chloride

Guidance literature:: Multi-step reaction with 2 steps

1: aqueous NaOH

2: benzene; SOCl₂

With sodium hydroxide; thionyl chloride; benzene;
DOI:10.1021/ja01615a032

Reference yield:

: 63-91-2,25191-15-5,658-69-5,67675-33-6
L-phenylalanine

: 2252-71-3
N-trifluoroacetyl-L-phenylalanine acid chloride

Guidance literature:: Multi-step reaction with 2 steps

1: 84 percent / KOMe / methanol / 40 °C

2: Vilsmeier reagent / various solvent(s) / 3 h / -12 - -10 °C

With potassium methanolate; Vilsmeier reagent; In methanol;
DOI:10.1016/j.tet.2003.02.002