18800-51-6

Basic information

• Product Name: 2,3-dimethylbenzenethiol
• Synonyms: 2,3-dimethylbenzenethiol;Benzenethiol, 2,3-dimethyl-;Einecs 242-586-2;2,3-Dimethyl Thiophe;Benzenethiol, dimethyl-
• CAS NO: 18800-51-6
• Molecular Formula: C₈H₁₀S
• Molecular Weight: 138.23
• EINECS: 242-586-2
• Product Categories: Phenol&Thiophenol&Mercaptan
• Mol File: 18800-51-6.mol
• Article Data: 3

Chemical Properties

• Melting Point: -30°C (estimate)
• Boiling Point: 213.67°C (estimate)
• Flash Point: 84.645 °C
• Appearance: /
• Density: 1.0340
• Vapor Pressure: 0.199mmHg at 25°C
• Refractive Index: 1.5466 (estimate)
• PKA: 6.92±0.48(Predicted)
• CAS DataBase Reference: 2,3-dimethylbenzenethiol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-dimethylbenzenethiol(18800-51-6)
• EPA Substance Registry System: 2,3-dimethylbenzenethiol(18800-51-6)

Safety Data

• Hazardous Substances Data: 18800-51-6(Hazardous Substances Data)

Usage

Uses

Used in Flavor and Fragrance Industry:
2,3-dimethylbenzenethiol is used as a flavoring agent for its strong, characteristic odor, adding unique scents to food products.
Used in Pharmaceutical Industry:
2,3-dimethylbenzenethiol is used as a precursor in the synthesis of various pharmaceuticals, contributing to the development of new medications.
Used in Agrochemical Industry:
In the agrochemical sector, 2,3-dimethylbenzenethiol is utilized as a starting material for the production of different agrochemicals, aiding in the creation of effective pest control solutions.
Used in Perfumery:
2,3-dimethylbenzenethiol is employed as a component in perfumes, leveraging its strong and distinctive smell to create unique and long-lasting fragrances.

InChI:InChI=1/C8H10S/c1-6-4-3-5-8(9)7(6)2/h3-5,9H,1-2H3

Upstream product

• 55990-91-5 1,2-bis(2,3-dimethylphenyl)disulfane 
• 2905-31-9 2,3-dimethylbenzenesulfonyl chloride 
• 140-89-6 potassium ethyl xanthogenate 
• 89816-80-8 2,3-dimethylphenyl ethyl xanthate 
• 87-59-2 2,3-Dimethylaniline 

Downstream Products

• 239791-55-0 2,3-dimethylphenyl-3-nitro-2-pyridinylsulfide 
• 162135-77-5 S-(2,3-Dimethylphenyl) N,N,N',N'-tetramethylphosphorodiamidothioate 
• 3919-67-3 3,4,6,7-Tetramethyl-dibenzothiophen 
• 105337-76-6 3-(2,3-Dimethyl-phenylmercapto)-butan-2-on 
• 66794-10-3 1,2-dimethyl-3-(methylsulfanyl)benzene 
• 132594-96-8 α-(2,3-Dimethyl-phenylmercapto)-propionaldehyd-diethylacetal 
• 116889-83-9 1-Acetonylmercapto-2,3-dimethyl-benzol 
• 109596-54-5 (2,3-Dimethyl-phenylmercapto)-acetaldehyd-dimethylacetal 
• 1226-19-3 2,2',3,3'-Tetramethyl-6-nitro-diphenylsulfid 
• 58844-67-0 2-(2,3-dimethylphenylthio)benzoic acid 
• 76972-79-7 1-(2,3-Dimethyl-phenyl)-4-(2,3-dimethyl-phenylsulfanyl)-phthalazine 
• 76972-72-0 1-(2,3-Dimethyl-phenylsulfanyl)-4-p-tolyl-phthalazine 
• 76972-65-1 1-(2,3-Dimethyl-phenylsulfanyl)-4-phenyl-phthalazine 
• 89816-85-3 2-(2,3-dimethylphenylthio)cyclohexanone 

Relevant articles and documents

Synthesis method of substituted thiophenol (by machine translation)

The invention provides a method for synthesizing substituted thiophenol, which comprises the following steps of preparing compound V compound and NaHSO3 Or KHHSO3 Reaction synthesis IV compound, compound of formula IV and SO2 Reaction-synthesis III compounds of formula III are passed NaBH in NaOH solution. 4 Of formula II is reduced and the compound of formula II is acidified to give a compound of formula I. The method for synthesizing the substituted thiophenol has the advantages of greenness, high efficiency, easiness in industrial application and the like. (by machine translation)

ARYLTHIOETHERPYRIMIDINE AND ARYLOXYETHERPYRIMIDINE DERIVATIVES AND THEIR THERAPEUTIC USES

Pyrimidine compounds, compositions containing pyrimidine compounds and methods of using pyrimidine compounds for regulating the production and/or release of ?-amyloid in cells are provided. The compounds provide for alleviation and prevention of ?-amyloid production, release and/or plaque development as occurs in, e.g., Alzheimer's disease.

The Synthesis of All of the Dimethyldibenzothiophenes and Monoethyldibenzothiophenes

The synthesis of all four isomers of the monoethyldibenzothiophenes and all of the sixteen isomers of the dimethyldibenzothiophenes has been accomplished.