2937-81-7

Basic information

• Product Name: 2,5-DIAMINO-1,3,4-THIADIAZOLE
• Synonyms: 2,5-DIAMINO-1,3,4-THIADIAZOLE;OTAVA-BB BB7020410037;[1,3,4]Thiadiazole-2,5-diamine;4-thiadiazole,2,5-diamino-3;2,5-DIAMINO-1,3,4-THIADIAZOLE 5%;(5-amino-1,3,4-thiadiazol-2-yl)amine;1,3,4-Thiadiazole, 2,5-diamino-
• CAS NO: 2937-81-7
• Molecular Formula: C₂H₄N₄S
• Molecular Weight: 116.14
• Mol File: 2937-81-7.mol
• Article Data: 6

Chemical Properties

• Melting Point: 210 °C
• Boiling Point: 349.2 °C at 760 mmHg
• Flash Point: 165 °C
• Appearance: /
• Density: 1.661 g/cm³
• Vapor Pressure: 4.79E-05mmHg at 25°C
• Refractive Index: 1.778
• Storage Temp.: 2-8°C(protect from light)
• PKA: 6.69±0.10(Predicted)
• CAS DataBase Reference: 2,5-DIAMINO-1,3,4-THIADIAZOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-DIAMINO-1,3,4-THIADIAZOLE(2937-81-7)
• EPA Substance Registry System: 2,5-DIAMINO-1,3,4-THIADIAZOLE(2937-81-7)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• Hazardous Substances Data: 2937-81-7(Hazardous Substances Data)

Usage

General Description

2,5-DIAMINO-1,3,4-THIADIAZOLE is a chemical compound with the molecular formula C2H4N4S. It is a heterocyclic organic compound that contains both sulfur and nitrogen atoms in its five-membered ring structure. 2,5-DIAMINO-1,3,4-THIADIAZOLE is used in the synthesis of pharmaceuticals and agrochemicals, as well as in the manufacture of dyes and pigments. It has also been studied for its potential as a corrosion inhibitor in the oil and gas industry. Due to its versatile applications, 2,5-DIAMINO-1,3,4-THIADIAZOLE is of interest to researchers and industries seeking to develop new materials and products.

InChI:InChI=1/C2H4N4S/c3-1-5-6-2(4)7-1/h(H2,3,5)(H2,4,6)

Upstream product

• 20953-16-6 1-thiocarbamylthiocarbohydrazide 
• 13751-17-2 1-[amino-(2-chloro-benzoylhydrazono)-methyl]-thiosemicarbazide; hydrochloride 
• 13751-16-1 1-(amino-benzoylhydrazono-methyl)-thiosemicarbazide; hydrochloride 
• 2937-80-6 1-thiocarbamoyl-semicarbazide 
• 142-46-1 bithiourea 

Downstream Products

• 64403-76-5 2-(5-amino-2-imino-[1,3,4]thiadiazol-3-yl)-1-p-tolyl-propan-1-one 
• 31737-02-7 2-amino-7-methyl-5-oxo-5H-1,3,4-thiadiazolo<3,2-a>pyrimidine 
• 58488-43-0 2-(5-amino-2-imino-[1,3,4]thiadiazol-3-yl)-1-(4-nitro-phenyl)-ethanone 
• 28863-43-6 N-(5-amino-1,3,4-thiadiazol-2-yl)benzamide 
• 62235-57-8 N,N′-(1,3,4-thiadiazole-2,5-diyl)dibenzamide 
• 31736-97-7 2,5-Bis-1,3,4-thiadiazol 
• 16163-65-8 2-(5-amino-2-imino-[1,3,4]thiadiazol-3-yl)-1-phenyl-ethanone 
• 16163-66-9 2-(5-amino-2-imino-[1,3,4]thiadiazol-3-yl)-1-p-tolyl-ethanone 
• 17489-74-6 2-(5-amino-2-imino-[1,3,4]thiadiazol-3-yl)-1-(4-chloro-phenyl)-ethanone 
• 16163-61-4 2-(5-amino-2-imino-[1,3,4]thiadiazol-3-yl)-1-(4-bromo-phenyl)-ethanone 
• 16163-67-0 2-(5-amino-2-imino-[1,3,4]thiadiazol-3-yl)-1-(4-methoxy-phenyl)-ethanone 
• 3898-08-6 1,1-diphenylthiourea 
• 578-95-0 10H-acridin-9-one 

Relevant articles and documents

Synthesis and properties of diaminothiadiazoles

Refined synthetic procedure for preparation of 3,5-diamino-1,2,4- thiadiazole and 2,5-diamino-1,3,4-thiadiazole based on the reaction of dithiourea or amidinothiourea with hydrogen peroxide is developed. The optimal reagents ratio was found, and monitoring methods were developed. It resulted in the increase of the target product yield and in a shorter reaction time. On the basis of 2,5-diamino-1,3,4-thiadiazole the alkylsubstituted 1,3,4- diaminothiadiazolidines were synthesized. The compounds prepared were characterized by the elemental analysis data, the IR, 1H NMR, and electronic spectra, and also by mass spectrometry.

Synthesis and molecular docking of hybrids ionic azole Schiff bases as novel CDK1 inhibitors and anti-breast cancer agents: In vitro and in vivo study

Three new hybrid ionic vanillyl-azole-Schiff bases (IVASBs) have synthesized and their antitumor performances were assessed in vitro against MCF-7 cells and in vivo against Ehrlich solid tumor (EST). The high binding energy score of IVASB3?CDK1 (?3.43 kca

Composition of matter having bioactive properties

Particles of coordinated complex comprising a basic, hydrous polymer and a capacitance adding compound, as well as methods for their production, are described. These complexes exhibit a high degree of bioactivity making them suitable for a broad range of applications through their incorporation into conventional vehicles benefiting from antimicrobial and similar properties.