96426-60-7

Basic information

• Product Name: METHYL 4-FLUOROCINNAMATE 97% PREDOMIN&
• Synonyms: METHYL 4-FLUOROCINNAMATE,TRANS;3-(4-Fluorophenyl)-2-propenoic acid methyl ester;METHYL 4-FLUOROCINNAMATE 97% PREDOMIN&;Methyl 4-Fluorocinnamate;Methyl 4-fluorocinnamate, predominantly trans 97%
• CAS NO: 96426-60-7
• Molecular Formula: C₁₀H₉FO₂
• Molecular Weight: 180.1756632
• Product Categories: C10 to C11;Carbonyl Compounds;Esters
• Mol File: 96426-60-7.mol
• Article Data: 84

Chemical Properties

• Melting Point: 45-49 °C(lit.)
• Boiling Point: 251.7°C at 760 mmHg
• Flash Point: >230 °F
• Appearance: /
• Density: 1.165g/cm³
• Vapor Pressure: 0.0201mmHg at 25°C
• Refractive Index: 1.54
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: METHYL 4-FLUOROCINNAMATE 97% PREDOMIN&(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL 4-FLUOROCINNAMATE 97% PREDOMIN&(96426-60-7)
• EPA Substance Registry System: METHYL 4-FLUOROCINNAMATE 97% PREDOMIN&(96426-60-7)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 96426-60-7(Hazardous Substances Data)

Usage

General Description

METHYL 4-FLUOROCINNAMATE 97% PREDOMIN& is a chemical compound with a purity of 97% and is primarily composed of methyl 4-fluorocinnamate. It is commonly used in the fragrance industry as a flavoring agent and in the production of perfumes and cosmetics. METHYL 4-FLUOROCINNAMATE 97% PREDOMIN& is known for its sweet and floral aroma, making it a popular ingredient in various scented products. Additionally, it is also used in the pharmaceutical industry for its potential medicinal properties. Overall, METHYL 4-FLUOROCINNAMATE 97% PREDOMIN& is a versatile chemical with applications in both the fragrance and pharmaceutical industries.

InChI:InChI=1/C10H9FO2/c1-13-10(12)7-4-8-2-5-9(11)6-3-8/h2-7H,1H3/b7-4+

Upstream product

• 292638-85-8 acrylic acid methyl ester 
• 460-00-4 1-Bromo-4-fluorobenzene 
• 79-20-9 acetic acid methyl ester 
• 459-57-4 4-fluorobenzaldehyde 
• 67-56-1 methanol 
• 459-32-5 4-fluorocinnamic acid 
• 74-88-4 methyl iodide 
• 1779-58-4 (methyloxycarbonylmethyl)triphenylphosphonium bromide 
• 459-32-5 (E)-4-fluorocinnamic acid 
• 13565-08-7 (E)-3-(4-fluorophenyl)acryloyl chloride 
• 405-99-2 para-fluorostyrene 
• 352-33-0 1-Chloro-4-fluorobenzene 
• 766-98-3 1-ethynyl-4-fluorobenzene 
• 201230-82-2 carbon monoxide 

Downstream Products

• 893751-08-1 trans-methyl 2-(4-fluorophenyl)cyclopropanecarboxylate 
• 203718-08-5 methyl 2,3-dibromo-3-(4-fluorophenyl)propanoate 
• 349446-90-8 2-(4-fluorophenyl)-1,1,3-trimethoxy carbonyl propane 
• 1246517-81-6 5-(4-fluorophenyl)-1-(4-isopropylphenyl)pyrazolidin-3-one 
• 889449-78-9 5-(4-fluorophenyl)-1-phenylpyrazolidin-3-one 
• 889449-79-0 5-(4-fluorophenyl)-1-phenyl-3-hydroxypyrazole 
• 1338378-14-5 4-chloro-5-(4-fluorophenyl)-1-phenyl-1H-pyrazol-3-ol 
• 1353660-95-3 C₃₀H₃₇FN₄O₇ 
• 1353660-75-9 C₄₅H₆₃FN₄O₉ 
• 1353660-83-9 C₃₆H₄₅FN₄O₆ 
• 174729-15-8 (2S,3R)-methyl 3-(4-fluorophenyl)-2,3-dihydroxypropanoate 
• 1353660-38-4 (2S,3S)-methyl 3-azido-3-(4-fluorophenyl)-2-hydroxypropanoate 

Relevant articles and documents

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Oxidative esterification of alcohols by a single-side organically decorated Anderson-type chrome-based catalyst

The direct esterification of alcohols with non-noble metal-based catalytic systems faces great challenges. Here, we report a new chrome-based catalyst stabilized by a single pentaerythritol decorated Anderson-type polyoxometalate, [N(C4H9)4]3[CrMo6O18(OH)3C{(OCH2)3CH2OH}], which can realize the efficient transformation from alcohols to esters by H2O2oxidation in good yields and high selectivity without extra organic ligands. A variety of alcohols with different functionalities including some natural products and pharmaceutical intermediates are tolerated in this system. The chrome-based catalyst can be recycled several times and still keep the original configuration and catalytic activity. We also propose a reasonable catalytic mechanism and prove the potential for industrial applications.