Methyl clofenapate
- Product Name
- Methyl clofenapate
- CAS No.
- 21340-68-1
- Chemical Name
- Methyl clofenapate
- Synonyms
- Clofenapate;Methyl clofenapate;Methyl Clofenopate;Methyl 2-[(4'-chloro[1,1'-biphenyl]-4-yl)oxy]-2-methylpropanoate;Methyl 2-[(4'-chloro[1,1'-biphenyl]-4-yl)oxy]-2-methylpropanoate;2-[[4'-Chloro-1,1'-biphenyl-4-yl]oxy]-2-methylpropionic acid methyl ester;Propanoic acid, 2-[(4'-chloro[1,1'-biphenyl]-4-yl)oxy]-2-methyl-, methyl ester
- CBNumber
- CB41116966
- Molecular Formula
- C17H17ClO3
- Formula Weight
- 304.77
- MOL File
- 21340-68-1.mol
Methyl clofenapate Property
- Melting point:
- 90 °C
- Boiling point:
- 419.15°C (rough estimate)
- Density
- 1.1483 (rough estimate)
- refractive index
- 1.4585 (estimate)
- form
- Solid
- color
- White to off-white
- EPA Substance Registry System
- Propanoic acid, 2-[(4'-chloro[1,1'-biphenyl]-4-yl)oxy]-2-methyl-, methyl ester (21340-68-1)
N-Bromosuccinimide Price
- Product number
- API0012934
- Product name
- METHYL CLOFENAPATE
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $500.79
- Updated
- 2021/12/16
Methyl clofenapate Chemical Properties,Usage,Production
Uses
Methyl clofenapate (Clofenapate methyl ester; MCP) is a peroxisome proliferator, which can induce hypolipidemia, peroxisome proliferation, and hepatocarcinogenesis[1].
General Description
White powder.
Reactivity Profile
A halogenated ester derivative. Esters react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides.
Fire Hazard
Flash point data for Methyl clofenapate are not available; however, Methyl clofenapate is probably combustible.
References
[1] Cruciani V, et al., Comparative effects of clofibrate and methyl clofenapate on morphological transformation and intercellular communication of Syrian hamster embryo cells. Carcinogenesis. 1997 Apr;18(4):701-6. DOI:10.1093/carcin/18.4.701
Methyl clofenapate Preparation Products And Raw materials
Raw materials
Preparation Products
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