250609-29-1

Basic information

• Product Name: 2,3-DIMETHYL-5-BENZYL THIOPHENE
• Synonyms: 2,3-DIMETHYL-5-BENZYL THIOPHENE
• CAS NO: 250609-29-1
• Molecular Formula: C₁₃H₁₄S
• Molecular Weight: 202.32
• Mol File: 250609-29-1.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 295.4±9.0 °C(Predicted)
• Appearance: /
• Density: 1.060±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 2,3-DIMETHYL-5-BENZYL THIOPHENE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-DIMETHYL-5-BENZYL THIOPHENE(250609-29-1)
• EPA Substance Registry System: 2,3-DIMETHYL-5-BENZYL THIOPHENE(250609-29-1)

Safety Data

• Hazardous Substances Data: 250609-29-1(Hazardous Substances Data)

Usage

General Description

2,3-DIMETHYL-5-BENZYL THIOPHENE is a chemical compound that belongs to the class of thiophenes, which are aromatic heterocyclic compounds containing a sulfur atom. It is characterized by its molecular structure, which consists of a thiophene ring with two methyl groups and a benzyl group attached to it. 2,3-DIMETHYL-5-BENZYL THIOPHENE can be used in various chemical reactions and synthesis processes, and it has potential applications in the pharmaceutical and agrochemical industries. Additionally, it may exhibit certain biological activities and could be of interest for medicinal and research purposes. Overall, 2,3-DIMETHYL-5-BENZYL THIOPHENE is a versatile chemical that presents opportunities for exploration and application in different fields.

Upstream product

• 632-16-6 2,3-dimethylthiophene 
• 100-39-0 benzyl bromide 
• 250609-52-0 2,3-dimethyl-5-benzylfuran 

Downstream Products

• 250609-40-6 (2-benzyl-4,5-dimethyl-thiophen-3-yl)-(3-cyclopentyl-4-methoxy-phenyl)-methanone 
• 250609-35-9 (2-benzyl-4,5-dimethyl-thiophen-3-yl)-(4-methoxy-3,5-dimethyl-phenyl)-methanone 

Relevant articles and documents

Synthesis of thiophenes in a deep eutectic solvent: heterocyclodehydration and iodocyclization of 1-mercapto-3-yn-2-ols in a choline chloride/glycerol medium

The heterocyclodehydration and iodocyclization of readily available 1-mercapto-3-yn-2-ols has been performed in a deep eutectic solvent (DES), that is, ChCl/Gly (1:2 molar ratio; ChCl=choline chloride, Gly=glycerol), as a non-conventional green solvent. T

Benzothiophenes, benzofurans, and indoles useful in the treatment of insulin resistance and hyperglycemia

This invention provides compounds of Formula I having the structure E is S, SO, SO2, O, or NR1c; X is hydrogen, halogen, alkyl of 1-6 carbon atoms, alkenyl of 2-7 carbon atoms, CN, aryl, aralkyl of 6-12 carbon atoms, hydroxyalkyl of 1-6 carbon atoms, hydroxyaralkyl of 6-12 carbon atoms, perfluoroalkyl of 1-6 carbon atoms, alkoxy of 1-6 carbon atoms, aryloxy; arylalkoxy, nitro, amino, NR2R2a, NR2COR2a, cycloalkylamino of 3-8 carbon atoms, morpholino, alkylsulfanyl of 1-6 carbon atoms, arylsulfanyl, pyridylsulfanyl, 2-N,N-dimethylaminoethylsulfanyl, —OCH2CO2R2bor —COR2c; Z1and Z2are each, independently, hydrogen, halogen, CN, alkyl of 1-6 carbon atoms, aryl, aralkyl of 6-12 carbon atoms, cycloalkyl of 3-8 carbon atoms, nitro, amino, —NR1R1a, —NR1COR1a, cycloalkylamino of 3-8 carbon atoms, morpholino, or OR8, or Z1and Z2may be taken together as a diene unit having the formula —CH═CR9—CR10═CR11—; or a pharmaceutically acceptable salt thereof, which are useful in treating metabolic disorders related to insulin resistance or hyperglycemia.

Furans, benzofurans, and thiophenes useful in the treatment of insulin resistance and hyperglycemia

This invention provides compounds of Formula I having the structure: wherein R1, R2, R3, R4, R5, R6, R7, R8, W, X, Y, and Z are as defined in the specification, or a pharmaceutically acceptable salt thereof, which are useful in treating metabolic disorders related to insulin resistance or hyperglycemia.