3461-34-5

Basic information

• Product Name: "Methyl 3,3-diphenyl-2-propenoate
• Synonyms: "Methyl 3,3-diphenyl-2-propenoate
• CAS NO: 3461-34-5
• Molecular Formula: C₁₆H₁₄O₂
• Molecular Weight: 238.28116
• EINECS: -0
• Mol File: 3461-34-5.mol
• Article Data: 48

Chemical Properties

• Appearance: /
• CAS DataBase Reference: "Methyl 3,3-diphenyl-2-propenoate(CAS DataBase Reference)
• NIST Chemistry Reference: "Methyl 3,3-diphenyl-2-propenoate(3461-34-5)
• EPA Substance Registry System: "Methyl 3,3-diphenyl-2-propenoate(3461-34-5)

Safety Data

• Hazardous Substances Data: 3461-34-5(Hazardous Substances Data)

Usage

General Description

Methyl 3,3-diphenyl-2-propenoate is a chemical compound with the molecular formula C17H16O2. It is a colorless liquid with a fruity odor, commonly used as a flavor and fragrance ingredient in cosmetic and personal care products. "Methyl 3,3-diphenyl-2-propenoate is also used in the production of pharmaceuticals and as an intermediate in organic synthesis. Methyl 3,3-diphenyl-2-propenoate is known for its high purity and stability, making it an important building block in the chemical industry. Its versatile nature and wide range of applications make it a valuable compound in various industries.

Upstream product

• 119-61-9 benzophenone 
• 97-97-2 chloroacetaldehyde dimethyl acetal 
• 103-26-4 Methyl cinnamate 
• 98-80-6 phenylboronic acid 
• 105245-42-9 tert-butyl(1-methoxyvinyl)dimethylsilane 
• 96-32-2 bromoacetic acid methyl ester 
• 5927-18-4 trimethyl phosphonoacetate 
• 530-48-3 1,1-Diphenylethylene 
• 101595-16-8 methyl 3-methoxy-3,3-diphenylpropanoate 
• 6294-89-9 hydrazinecarboxylic acid methyl ester 
• 621-82-9 Cinnamic acid 
• 98-09-9 benzenesulfonyl chloride 
• 103-26-4 methyl cinnamate 
• 1067-74-9 Methyl diethylphosphonoacetate 

Downstream Products

• 57090-79-6 1,1,4,4-tetraphenyl-3-buten-2-one 
• 10338-20-2 2-(3,3-Diphenyl-propen-2-yl)-3-phytyl-naphthochinon-1,4 
• 10338-00-8 2-(3,3-Diphenyl-propen-2-yl)-1,4-diacetoxynaphthalin 
• 10338-19-9 2-(3,3-Diphenyl-propen-2-yl)-3-(3-methyl-buten-2-yl)-naphthochinon-1,4 
• 10337-99-2 2-(3,3-Diphenyl-propen-2-yl)-naphthochinon-1,4 
• 20797-50-6 3,3-bis-(4-nitro-phenyl)-acrylic acid 
• 252770-39-1 1-(3,3-dimethyl-2-oxo-pentanoyl)-piperidine-2-carbothioic acid S-(3,3-diphenyl-propyl) ester 
• 205388-30-3 3,3-diphenyl-1-propyl (2S)-1-(3,3-dimethyl-1,2-dioxopentyl)-2-pyrrolidinecarbothioate 
• 454484-95-8 3,3-diphenylpropane-1-thiol 
• 20017-68-9 1-bromo-3,3-diphenylpropane 

Relevant articles and documents

Reactions of vinyl type carbocations generated in fluorosulfonic acid with benzene derivatives. New synthesis of alkyl 3,3-diarylpropenoates

Vinyl type carbocations ArC+=CHX [X = CO2H, CO 2Alk, C≡N, P(O)(OAlk)2] generated from alkyl 3-arylpropynoates and related compounds in fluorosulfonic acid at -75 to -20°C react with various benzene derivatives,

MALIC ENZYME INHIBITORS

The present invention relates to novel compounds useful as malic enzyme (ME) inhibitors, processes for their preparation and use of these compounds for the therapeutic treatment of disorders mediated by ME such as cancers (e.g. pancreatic ductal adenocarcinoma (PDAC)) in humans.

Rh-Catalyzed Direct Carboxylation of Alkenyl C?H Bonds of Alkenylpyrazoles

The Rh-catalyzed direct carboxylation of alkenyl C?H bonds was achieved by using pyrazole as a removable directing group. In the presence of 5 mol% RhCl3 ? 3H2O, 6 mol% P(Mes)3, and 2 equiv. of AlMe2(OMe), the alkenyl C?H bond of various alkenylpyrazoles was directly carboxylated in good yields under CO2 atmosphere. Furthermore, several useful transformations of the pyrazole moiety of the product were achieved to afford synthetically useful carboxylic acid derivatives in good yields.