HALOFENATE

Base Information

Chemical Name:HALOFENATE
CAS No.:26718-25-2
Molecular Formula:C₁₉H₁₇ClF₃NO₄
Molecular Weight:415.796
Hs Code.:
Mol file:26718-25-2.mol

Synonyms:Aceticacid, (p-chlorophenyl)[(a,a,a-trifluoro-m-tolyl)oxy]-, ester withN-(2-hydroxyethyl)acetamide (8CI); Acetamide, N-(2-hydroxyethyl)-,(p-chlorophenyl)[(a,a,a-trifluoro-m-tolyl)oxy]acetate (ester) (8CI);(p-Chlorophenyl)[(a,a,a-trifluoro-m-tolyl)oxy]acetic acid ester withN-(2-hydroxyethyl)acetamide; 2-Acetamidoethyl(p-chloro-phenyl)-(m-trifluoromethyl-phenoxy)acetate; 2-Acetamidoethyl4-Chlorophenyl(3-trifluoromethylphenoxy)acetate; Halofenate; Lipivas; MK 185

Suppliers and Price of HALOFENATE

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

TRC
Halofenate
25mg
$ 1350.00

American Custom Chemicals Corporation
HALOFENATE 95.00%
5MG
$ 504.38

Total 6 raw suppliers

Chemical Property of HALOFENATE

Chemical Property:

Vapor Pressure:3.44E-12mmHg at 25°C
Melting Point:93.5 - 95.5 °C
Boiling Point:551.1°Cat760mmHg
PKA:15.32±0.46(Predicted)
Flash Point:287.1°C
PSA：64.63000
Density:1.331g/cm³
LogP:4.54910

Purity/Quality:

99% ^*data from raw suppliers

Halofenate ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses Antihyperlipoproteinemic; uricosuric. Halofenate is a selective peroxisome proliferator-activated receptor γ (PPARγ) modulator with antidiabetic activity.

Technology Process of HALOFENATE

There total 2 articles about HALOFENATE 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:

: N-acetylaminoethyl 2-bromo-2-(4-chlorophenyl)acetate

: 98-17-9
3-Trifluoromethylphenol

: 24136-23-0,24136-24-1,26718-25-2
2-acetamidoethyl (3-trifluoromethylphenoxy)(4-chlorophenyl)acetate

Guidance literature:: With potassium hydroxide; In isopropyl alcohol; at 20 ℃; for 4h;

Reference yield:

: 24136-23-0,24136-24-1,26718-25-2
2-acetamidoethyl (3-trifluoromethylphenoxy)(4-chlorophenyl)acetate

Guidance literature:: entspr. Acetat, Acetamidoethanol;

Reference yield:

: 24136-23-0,24136-24-1,26718-25-2
2-acetamidoethyl (3-trifluoromethylphenoxy)(4-chlorophenyl)acetate

: 4687-08-5,23953-40-4
halofenic acid

Guidance literature:: 2-acetamidoethyl (3-trifluoromethylphenoxy)(4-chlorophenyl)acetate; With sodium hydroxide; In water; at 60 ℃; for 1h;

With hydrogenchloride; In water; 1,2-dichloro-ethane; at 29 - 40 ℃; pH=0.85;