35066-32-1

Basic information

• Product Name: Methyl 3-cyano-4-Methylbenzoate
• Synonyms: Methyl 3-cyano-4-Methylbenzoate;5-cyano-4-Methylbenzoic acid Methyl ester;3-Cyano-4-methyl-methylbenzoate;3-Cyano-4-methyl-benzoic acid methyl ester;Methyl3-cyano-4-Methylbenzoate35066-32-1
• CAS NO: 35066-32-1
• Molecular Formula: C₁₀H₉NO₂
• Molecular Weight: 175.18396
• Mol File: 35066-32-1.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 289.2°C at 760 mmHg
• Flash Point: 132.4°C
• Appearance: /
• Density: 1.15g/cm³
• Vapor Pressure: 0.00224mmHg at 25°C
• Refractive Index: 1.53
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: Methyl 3-cyano-4-Methylbenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl 3-cyano-4-Methylbenzoate(35066-32-1)
• EPA Substance Registry System: Methyl 3-cyano-4-Methylbenzoate(35066-32-1)

Safety Data

• Hazardous Substances Data: 35066-32-1(Hazardous Substances Data)

Usage

General Description

Methyl 3-cyano-4-Methylbenzoate is a chemical compound with the molecular formula C11H11NO2. It is a methyl ester of 3-cyano-4-methylbenzoic acid, and it is commonly used as a flavoring agent in the food and beverage industry. Methyl 3-cyano-4-Methylbenzoate has a yellowish crystalline appearance and a sweet, fruity odor. It is often used in the synthesis of pharmaceuticals and agrochemicals, and it also has applications in organic synthesis and as an intermediate in the production of various other chemicals. Methyl 3-cyano-4-Methylbenzoate is considered to be relatively stable and has low toxicity, making it suitable for a wide range of industrial and commercial uses.

InChI:InChI=1/C10H9NO2/c1-7-3-4-8(10(12)13-2)5-9(7)6-11/h3-5H,1-2H3

Upstream product

• 186581-53-3 diazomethane 
• 2458-12-0 3-amino-p-toluic acid 
• 151-50-8 potassium cyanide 
• 1943-88-0 2,4-dicyanotoluene 
• 96-98-0 4-methyl-3-nitrobenzoic acid 
• 104901-43-1 methyl 3-bromo-4-methylbenzoate 
• 2417-72-3 Methyl 4-(bromomethyl)benzoate 
• 19158-51-1 P-toluenesulfonyl cyanide 
• 18595-18-1 3-amino-4-methyl benzoic acid methyl ester 
• 90347-66-3 methyl 3-iodo-4-methylbenzoate 
• 7697-26-9 3-bromo-4-methylbenzoic acid 
• 557-21-1 zinc(II) cyanide 

Downstream Products

• 23038-61-1 dimethyl 4-methylbenzene-1,3-dicarboxylate 
• 219519-17-2 4-bromomethyl-3-cyanobenzoic acid methyl ester 

Relevant articles and documents

Enhanced accuracy of single-molecule diffusion measurements with a photocleavable energy-transfer dyad

A photocleavable energy-transfer dyad was synthesized, characterized, and applied to single-molecule fluorescence microscopy. After photocleavage, a combination of independent two-color single-molecule tracking and analysis of single-molecule energy-transfer efficiencies allows the determination of the temporal evolution of the relative distances between both fragments from the nm to the μm scale. This gives access to a broad range of diffusion coefficients. Copyright

BIARYLOXY DERIVATIVES AS TTX-S BLOCKERS

The present invention relates to biaryloxy derivatives which have blocking activities of voltage gated sodium channels as the TTX-S channels, and which are useful in the treatment or prevention of disorders and diseases in which voltage gated sodium channel is involved.　The invention also relates to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which voltage gated sodium channels are involved.

THERAPEUTIC INHIBITORY COMPOUNDS

The invention provides compounds of Formula I and Formula II: A-B-C-D-E-F-G-J (I) C-D-E-F-G-J (II) wherein A, B, C, D, E, F, G, and J have any of the values defined in the specification, and salts thereof. The compounds are useful for inhibiting plasma kallikrein, and for treating a disease or condition in an animal where inhibition of plasma kallikrein is indicated.