1001055-67-9

Basic information

• Product Name: 4-CYANO-3,5-DIMETHYL-BENZOIC ACID METHYL ESTER
• Synonyms: 4-CYANO-3,5-DIMETHYL-BENZOIC ACID METHYL ESTER;METHYL 4-CYANO-3,5-DIMETHYLBENZOATE
• CAS NO: 1001055-67-9
• Molecular Formula: C₁₁H₁₁NO₂
• Molecular Weight: 189.21054
• Mol File: 1001055-67-9.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-CYANO-3,5-DIMETHYL-BENZOIC ACID METHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 4-CYANO-3,5-DIMETHYL-BENZOIC ACID METHYL ESTER(1001055-67-9)
• EPA Substance Registry System: 4-CYANO-3,5-DIMETHYL-BENZOIC ACID METHYL ESTER(1001055-67-9)

Safety Data

• Hazardous Substances Data: 1001055-67-9(Hazardous Substances Data)

Usage

General Description

4-CYANO-3,5-DIMETHYL-BENZOIC ACID METHYL ESTER is a chemical compound with the molecular formula C11H11NO2. It is an ester of 4-cyano-3,5-dimethylbenzoic acid and methanol. 4-CYANO-3,5-DIMETHYL-BENZOIC ACID METHYL ESTER is commonly used in the flavor and fragrance industry as a raw material for the synthesis of various aromatic compounds. It is also used in the production of pharmaceuticals and agrochemicals. Additionally, this chemical has been studied for its potential anti-inflammatory and antioxidant properties. Overall, 4-CYANO-3,5-DIMETHYL-BENZOIC ACID METHYL ESTER is a versatile compound with applications in various industries and potential therapeutic benefits.

Upstream product

• 432022-88-3 4-bromo-3,5-dimethylbenzoic acid methyl ester 
• 544-92-3 copper(I) cyanide 
• 557-21-1 zinc(II) cyanide 
• 5471-81-8 methyl 4-iodo-3-methylbenzoate 
• 80-48-8 methyl p-toluene sulfonate 

Downstream Products

• 1378861-92-7 C₁₀H₁₁NO 

Relevant articles and documents

Modular Dual-Tasked C-H Methylation via the Catellani Strategy

We report a dual-tasked methylation that is based on cooperative palladium/norbornene catalysis. Readily available (hetero)aryl halides (39 iodides and 4 bromides) and inexpensive MeOTs or trimethylphosphate are utilized as the substrates and methylating reagent, respectively. Six types of "ipso" terminations can modularly couple with this "ortho" C-H methylation to constitute a versatile methylation toolbox for preparing diversified methylated arenes. This toolbox features inexpensive methyl sources, excellent functional-group tolerance, simple reaction procedures, and scalability. Importantly, it can be uneventfully extended to isotope-labeled methylation by switching to the corresponding reagents CD3OTs or 13CH3OTs. Moreover, this toolbox can be applied to late-stage modification of biorelevant substrates with complete stereoretention. We believe these salient and practical features of our dual-tasked methylation toolbox will be welcomed by academic and industrial researchers.