1795-04-6

Basic information

• Product Name: 2,3,5-TRIMETHYLTHIOPHENE
• Synonyms: 2,3,4-Trimethylthiophene;Trimethylthiophene;2,3,5-TRIMETHYLTHIOPHENE 97+%
• CAS NO: 1795-04-6
• Molecular Formula: C₇H₁₀S
• Molecular Weight: 126.2193
• EINECS: 217-268-1
• Mol File: 1795-04-6.mol
• Article Data: 8

Chemical Properties

• Melting Point: -26.2°C
• Boiling Point: 82°C 51mm
• Appearance: /
• Density: 0,98 g/cm3
• Refractive Index: 1.5183
• CAS DataBase Reference: 2,3,5-TRIMETHYLTHIOPHENE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,5-TRIMETHYLTHIOPHENE(1795-04-6)
• EPA Substance Registry System: 2,3,5-TRIMETHYLTHIOPHENE(1795-04-6)

Safety Data

• Statements: 10-36/37/38
• Safety Statements: 16-36/37/39
• RIDADR: 1993
• Hazardous Substances Data: 1795-04-6(Hazardous Substances Data)

Usage

General Description

2,3,5-Trimethylthiophene is a chemical compound with the molecular formula C7H8S. It is a colorless to pale yellow liquid with a strong, sweet odor. 2,3,5-Trimethylthiophene is mainly used as a building block in the synthesis of pharmaceuticals and agrochemicals. It is also used in the production of fragrances and flavorings. Additionally, it has applications in the manufacturing of polymers and as a chemical intermediate in organic synthesis. The compound is known for its potential as a fragrance and is considered to be an aromatic compound with an appealing aroma. However, it should be handled and stored with care, as it may pose health and environmental risks if not managed properly.

Upstream product

• 188290-36-0 thiophene 
• 624-92-0 Dimethyldisulphide 
• 14503-51-6 tetramethylthiophene 
• 343268-79-1 3,4-dimethylthiophene-2-carbaldehyde 
• 3141-25-1 2,3,4-tribromothiophene 
• 632-15-5 3,4-dimethylthiophene 
• 169328-87-4 2-bromo-3,4-dimethylthiophene 
• 74-88-4 methyl iodide 
• 3141-26-2 3,4-dibromothiophene 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 1451066-43-5 trimethyl-2-(2,4,6-trimethylphenyl)thiophene 
• 188290-36-0 thiophene 
• 632-16-6 2,3-dimethylthiophene 
• 14503-51-6 tetramethylthiophene 

Relevant articles and documents

Synthesis and structure of novel disulfide(trisulfide)-containing thiophenes

A novel trisulfide-containing thiophene, 1,5-dihydrothieno[3,4-e][1,2,3] trithiepine (5), and a disulfide analogue, 1,4-dihydrothieno[3,4-d][1,2]dithiine (4), were designed and synthesized. All the compounds were characterized by FT-IR, NMR, Raman, MS, an

Reaction of dimethyl disulfide with thiophene catalyzed by zeolite

Reaction of dimethyl disulfide with thiophene under the action of highly siliceous zeolite at 180-350°C and contact time 0.6-14 s resulted in formation of thioalkylation products, 2-(methylsulfanyl)- and 2,5-bis(methylsulfanyl)thiophenes and also alkylate

In vivo phenotypic drug discovery: Applying a behavioral assay to the discovery and optimization of novel antipsychotic agents

Phenotypic drug discovery (PDD) is increasingly being recognized as a viable compliment to target-based drug discovery (TDD). By measuring functional changes, typically at a systems level, PDD can facilitate the identification of compounds having a desirable pharmacology. This capability is particularly important when studying CNS diseases where drug efficacy may require modulation of multiple targets in order to overcome a robust, adaptive biological system. Here, we report the application of a mouse-based high-dimensional behavioral assay to the discovery and optimization of a structurally and mechanistically novel antipsychotic. Lead optimization focused on optimizing complex behavioral features and no explicit effort was made to identify the target (or targets) involved.