117379-97-2

Basic information

• Product Name: methyl 2-methyl-1-benzofuran-5-carboxylate
• Synonyms: methyl 2-methyl-1-benzofuran-5-carboxylate;2-methyl-5-benzofurancarboxylic acid methyl ester;2-methylbenzofuran-5-carboxylic acid methyl ester;methyl 2-methylbenzofuran-5-carboxylate
• CAS NO: 117379-97-2
• Molecular Formula: C₁₁H₁₀O₃
• Molecular Weight: 190.1953
• Mol File: 117379-97-2.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: methyl 2-methyl-1-benzofuran-5-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2-methyl-1-benzofuran-5-carboxylate(117379-97-2)
• EPA Substance Registry System: methyl 2-methyl-1-benzofuran-5-carboxylate(117379-97-2)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 117379-97-2(Hazardous Substances Data)

Usage

General Description

Methyl 2-methyl-1-benzofuran-5-carboxylate is an organic compound with the chemical formula C12H12O3. It is a colorless to pale yellow liquid with a floral, fruity odor. methyl 2-methyl-1-benzofuran-5-carboxylate is commonly used as a fragrance ingredient in the production of perfumes, soaps, and cosmetics due to its pleasant scent. Methyl 2-methyl-1-benzofuran-5-carboxylate is also used in the pharmaceutical industry as an intermediate in the synthesis of various drugs. Additionally, it has potential applications in the field of organic synthesis and as a flavoring agent in food products. methyl 2-methyl-1-benzofuran-5-carboxylate should be handled and stored with care due to its flammability and potential health hazards.

Upstream product

• 64-18-6 formic acid 
• 219763-06-1 2-Methyl-1-benzofuran-5-carboxylic acid 
• 53596-60-4 methyl 3-allyl-4-hydroxybenzoate 
• 25016-01-7 5-bromo-2-methoxybenzaldehyde 
• 15804-76-9 3-(2-nitropropen-1-yl)-4-methoxybromobenzene 
• 1334637-58-9 C₁₁H₁₁ClO₃ 
• 205826-73-9 (5-Bromo-2-methoxyphenyl)acetone 
• 54965-04-7 5-bromo-2-methylbenzo[b]furan 
• 1761-61-1 5-bromosalicyclaldehyde 
• 67-56-1 methanol 
• 99-76-3 methyl 4-hydroxylbenzoate 
• 35750-24-4 methyl 4-allyloxybenzoate 
• 98260-05-0 methyl 4-(2-propynoxy)benzoate 

Downstream Products

• 219763-06-1 2-Methyl-1-benzofuran-5-carboxylic acid 
• 219764-11-1 3-(4-bromo-2-chlorobenzyl)-5-(methoxycarbonyl)-2-methylbenzo[b]furan 
• 219763-10-7 5-carboxy-3-(2,4-dichlorobenzyl)-2-methylbenzo[b]furan 
• 219764-14-4 3-(4-bromo-2-chlorobenzyl)-5-carboxy-2-methylbenzo[b]furan 
• 219763-17-4 5-carboxy-2-methyl-3-(4-phenylbenzyl)benzo[b]furan 
• 219764-13-3 5-carboxy-3-(2-chloro-4-phenylbenzyl)-2-methylbenzo[b]furan 

Relevant articles and documents

Enantio- and Diastereoselective, Complete Hydrogenation of Benzofurans by Cascade Catalysis

We report an enantio- and diastereoselective, complete hydrogenation of multiply substituted benzofurans in a one-pot cascade catalysis. The developed protocol facilitates the controlled installation of up to six new defined stereocenters and produces architecturally complex octahydrobenzofurans, prevalent in many bioactive molecules. A unique match of a chiral homogeneous ruthenium-N-heterocyclic carbene complex and an in situ activated rhodium catalyst from a complex precursor act in sequence to enable the presented process.

HETEROCYCLIC COMPOUNDS FOR THE INHIBITION OF PASK

Disclosed herein are new heterocyclic compounds and compositions and their application as pharmaceuticals for the treatment of disease. Methods of inhibiting PAS Kinase (PASK) activity in a human or animal subject are also provided for the treatment of diseases such as diabetes mellitus.

Cesium Fluoride-Mediated Claisen Rearrangements of Phenyl Propargyl Ethers: Effect of a Substituent on the Phenyl Ring on the Rearrangement

Methoxy or methoxycarbonyl-substituted phenyl propargyl ethers were subjected to Claisen rearrangement either in the absence or in the presence of CsF.Substituent effect on the cyclization is discussed.