36596-67-5

Basic information

• Product Name: ETHYL 2,6-DIMETHYLBENZOATE
• Synonyms: RARECHEM AL BI 0363;ETHYL 2,6-DIMETHYLBENZOATE;2,6-Dimethylbenzoic acid ethyl ester
• CAS NO: 36596-67-5
• Molecular Formula: C₁₁H₁₄O₂
• Molecular Weight: 178.23
• Product Categories: Aromatic Esters
• Mol File: 36596-67-5.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 78-80°C 0,9mm
• Flash Point: 78-80°C/0.9mm
• Appearance: liquid
• Density: 1.01 g/cm³
• Vapor Pressure: 0.0502mmHg at 25°C
• Refractive Index: 1.4980
• Solubility: Difficult to mix.
• BRN: 2575407
• CAS DataBase Reference: ETHYL 2,6-DIMETHYLBENZOATE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL 2,6-DIMETHYLBENZOATE(36596-67-5)
• EPA Substance Registry System: ETHYL 2,6-DIMETHYLBENZOATE(36596-67-5)

Safety Data

• Safety Statements: 24/25
• Hazardous Substances Data: 36596-67-5(Hazardous Substances Data)

Usage

General Description

ETHYL 2,6-DIMETHYLBENZOATE is a chemical compound with the molecular formula C11H14O2. It is an ester, specifically the ethyl ester of 2,6-dimethylbenzoic acid. ETHYL 2,6-DIMETHYLBENZOATE is a colorless liquid with a fruity odor and is commonly used as a fragrance ingredient in various cosmetic and personal care products. It is also used as a flavoring agent in food products. Additionally, ETHYL 2,6-DIMETHYLBENZOATE has been studied for its potential anti-inflammatory and antioxidant properties, making it a subject of interest in the field of medicinal chemistry. Overall, this chemical compound has a range of industrial and scientific applications, primarily due to its fragrance and flavoring properties and potential bioactivity.

InChI:InChI=1/C11H14O2/c1-4-13-11(12)10-8(2)6-5-7-9(10)3/h5-7H,4H2,1-3H3

Upstream product

• 632-46-2 2,6-dimethylbenzoic acid 
• 75-03-6 ethyl iodide 
• 64-17-5 ethanol 
• 541-41-3 chloroformic acid ethyl ester 
• 21450-64-6 (2,6-dimethylphenyl)magnesium bromide 
• 21900-37-8 2,6-dimethylbenzoyl chloride 
• 78-39-7 Triethyl orthoacetate 

Downstream Products

• 635316-53-9 2-bromomethyl-6-methyl-benzoic acid ethyl ester 
• 62285-58-9 2,6-dimethylbenzyl alcohol 
• 113597-93-6 ethyl 2,6-bis((3,5-bis((diphenylmethoxy)carbonyl)phenoxy)methyl)benzoate 
• 113585-37-8 ethyl 2,6-bis((3,5-dicarboxyphenoxy)methyl)benzoate 
• 113585-42-5 2,6-Bis-(3,5-bis-chlorocarbonyl-phenoxymethyl)-benzoic acid ethyl ester 
• 113585-50-5 ethyl 2,6-bis(bromomethyl)benzoate 

Relevant articles and documents

Pyridazone derivative and its uses

The present invention belongs to the pharmaceutical field, specifically relates to a pyridazone derivative and its uses, compounds thereof and pharmaceutically acceptable salts, solvates including hydrates, polycrystallines, prodrugs, co-crystallines, tau

A new versatile synthesis of esters from Grignard reagents and chloroformates

Cross-coupling reactions of chloroformates with organocopper reagents, derived from Grignard reagents, cuprous bromide and lithium bromide, provide a rapid and straightforward method for the synthesis of esters. Georg Thieme Verlag Stuttgart.

Synthesis, Characterization, and X-ray Structure of the Ruthenium "Picnic-Basket" Porphyrins

The synthesis and characterization of a new class of sterically protected porphyrins, the "picnic-basket" porphyrins, are presented.These tetraarylporphyrins, which were prepared as cytochrome P-450 active-site analogues, bear a rigid superstucture on one face of the porphyrin macrocycle.The cavity defined by the appended superstructure may be readily varied in size, chirality, and functionality.In addition, the synthesis and characterization, including an X-ray structure, of several ruthenium picnic-basket porphyrin carbonyl complexes are reported.The regiochemistry of axial ligation in these ruthenium derivatives has been determined by 1H NMR spectroscopy.