3418-46-0

Basic information

• Product Name: 1,3-dimethylbenzimidazoline-2-thione
• Synonyms: 1,3-dimethylbenzimidazoline-2-thione
• CAS NO: 3418-46-0
• Molecular Formula: C₉H₁₀N₂S
• Molecular Weight: 178.25
• Mol File: 3418-46-0.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 270.8°Cat760mmHg
• Flash Point: 117.6°C
• Appearance: /
• Density: 1.28g/cm³
• Vapor Pressure: 0.0067mmHg at 25°C
• Refractive Index: 1.698
• CAS DataBase Reference: 1,3-dimethylbenzimidazoline-2-thione(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-dimethylbenzimidazoline-2-thione(3418-46-0)
• EPA Substance Registry System: 1,3-dimethylbenzimidazoline-2-thione(3418-46-0)

Safety Data

• Hazardous Substances Data: 3418-46-0(Hazardous Substances Data)

Usage

General Description

1,3-dimethylbenzimidazoline-2-thione is a chemical compound with the molecular formula C9H10N2S. It is a heterocyclic compound that contains a benzene ring fused to an imidazole ring, with a sulfur atom and two methyl groups attached. 1,3-dimethylbenzimidazoline-2-thione is commonly used as a reagent in organic synthesis and as a ligand in coordination chemistry. It has been studied for its potential pharmaceutical applications, particularly as an anti-cancer and anti-inflammatory agent. Additionally, 1,3-dimethylbenzimidazoline-2-thione has been investigated for its antioxidant properties and its ability to inhibit the growth of bacteria and fungi.

InChI:InChI=1/C9H10N2S/c1-10-7-5-3-4-6-8(7)11(2)9(10)12/h3-6H,1-2H3

Upstream product

• 110-86-1 pyridine 
• 186581-53-3 diazomethane 
• 583-39-1 2,3-dihydrobenzimidazol-2-thione 
• 60-29-7 diethyl ether 
• 555-31-7 aluminum isopropoxide 

Downstream Products

• 78864-26-3 C₁₆H₁₇N₃O₂S₂ 

Relevant articles and documents

METHOD FOR ALKYLATING A MOLECULE OR AN ION

The present invention relates to a method for alkylating a molecule or an ion, wherein the molecule or the ion is alkylated by reacting it with an alkylating agent, wherein the alkylating agent is a compound according to formula (1) or a compound according to formula (4). In the formulae (1) and (4), R1 is a substituted C1-20-alkyl group, an unsubstituted C1-20-alkyl group, a substituted C3-20-cycloalkyl group or an unsubstituted C3-20-cycloaalkyl group, R2 is a substituted or unsubstituted C1-20 hydrocarbon residue or a hydrogen atom, R3 is a substituted or unsubstituted C1-20 hydrocarbon residue or a hydrogen atom, R4 and R5 are linked with each other to form an aromatic group or are independently from each other selected from the group consisting of a hydrogen atom, substituted and unsubstituted C1-20 hydrocarbon residues and electron withdrawing groups, R10 to R13 are independently from each other selected from the group consisting of a hydrogen atom, a substituted C1-20-alkyl group, an unsubstituted C1-20-alkyl group, a substituted C3-20-cycloalkyl group and an unsubstituted C3-20-cycloaalkyl group and A- is an anion.