36988-21-3

Basic information

• Product Name: 1,2,4-Thiadiazole-5(2H)-thione, 3-methyl-
• Synonyms: 1,2,4-Thiadiazole-5(2H)-thione, 3-methyl-;3-Methyl-1,2,4-thiadiazole-5(2H)-thione
• CAS NO: 36988-21-3
• Molecular Formula: C3H4 N2 S2
• Molecular Weight: 132.21
• Mol File: 36988-21-3.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 182.9°Cat760mmHg
• Flash Point: 64.4°C
• Appearance: /
• Density: 1.58g/cm³
• Vapor Pressure: 0.791mmHg at 25°C
• Refractive Index: 1.774
• CAS DataBase Reference: 1,2,4-Thiadiazole-5(2H)-thione, 3-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,4-Thiadiazole-5(2H)-thione, 3-methyl-(36988-21-3)
• EPA Substance Registry System: 1,2,4-Thiadiazole-5(2H)-thione, 3-methyl-(36988-21-3)

Safety Data

• Hazardous Substances Data: 36988-21-3(Hazardous Substances Data)

Usage

Type of Compound

Heterocyclic compound

Molecular Weight

120.16 g/mol

Melting Point

119-120 degrees Celsius

Composition

Contains carbon (C), hydrogen (H), nitrogen (N), and sulfur (S)

Industrial Applications

Used in various industrial applications

Antimicrobial Properties

Known for its antimicrobial properties

Antifungal Properties

Known for its antifungal properties

Pharmaceutical Use

Useful in the production of pharmaceuticals

Agricultural Use

Useful in the production of agricultural products

Antioxidant Potential

Has been studied for its potential use as an antioxidant

Material Development

Studied for the development of materials for industrial applications

InChI:InChI=1/C3H4N2S2/c1-2-4-3(6)7-5-2/h1H3,(H,4,5,6)

Upstream product

• 143-37-3 acetamidine 
• 21734-85-0 5-chloro-3-methyl-1,2,4-thiazole 
• 17356-08-0 thiourea 

Downstream Products

• 32991-51-8 3-Methyl-1,2,4-thiadiazol-5-ylthioessigsaeure 
• 66961-61-3 3-methyl-5-(1-methyl-5-nitro-1H-imidazol-2-ylmethylsulfanyl)-[1,2,4]thiadiazole 

Relevant articles and documents

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Oxazoles and their agricultural compositions

A compound having the formula R--S(O)n CH2 CH2 CH=CF2, wherein R is a phenyl group or a heterocyclic group selected from furyl, thienyl, isoxazolyl, isothiazolyl, oxazolyl, thiazolyl, imidazolyl, pyrazolyl, 1,2,4-oxadiazolyl, 1,2,4-thiadiazolyl, 1,3,4-oxadiazolyl, 1,3,4-thidiazolyl, tetrazolyl, pyridyl, pyridazinyl, pyrazinyl, 1,2,3-triazinyl, 1,3,4-triazinyl, and 1,3,5-triazinyl groups, said phenyl or heterocyclic group being optionally substituted by optionally substituted alkyl, optionally substituted alkenyl, alkynyl, cycloalkyl, alkylcycloalkyl, alkoxy, alkenyloxy, alkynyloxy, hydroxyalkyl, alkoxyalkyl, optionally substituted aryl, optionally substituted arylalkyl, optionally substituted heteroaryl, optionally substituted heteroarylalkyl, optionally substituted aryloxy, optionally substituted arylalkoxy, optionally substituted aryloxyalkyl, optionally substituted heteroaryloxy, optionally substituted heteroarylalkoxy, optionally substituted heteroaryloxyalkyl, haloalkyl, haloalkenyl, haloalkynyl, haloalkoxy, haloalkenyloxy, haloalkynyloxy, halogen, hydroxy, cyano, nitro, --NR7R8, --NR7COR8, --NR7CSR8, --NR7SO2R8, --N(SO2R7)(SO2R8), --COR7, --CONR7R8, -alkylCONR7R8, --CR7NR8, --COOR7, --OCOR7, --SR7, --SOR7, --SO2R7, -alkylSR7, -alkylSOR7, -alkylSO2R7, --OSO2R7, --SO2NR7R8, --CSNR7R8, --SiR7R8R9, --OCH2CO2R7, --OCH2CH2CO2R7, --CONR7SO2R8, -alkylCONR7SO2R8, --NHCONR7R8, --NHCSNR7R8, or an adjacent pair of R1, R2, R3, R4, R5 and R6 when taken together form a fused 5- or 6-membered carbocyclic or heterocyclic ring; R7, R8 and R9 are each independently hydrogen, optionally substituted alkyl, optionally substituted alkenyl, alkynyl, optionally substituted aryl or optionally substituted arylalkyl, haloalkyl, haloalkenyl, haloalkynyl, halogen or hydroxy.