30843-69-7

Basic information

• Product Name: 1,3,4-Thiadiazole-2,5-dithioacetic acid
• Synonyms: 1,3,4-Thiadiazole-2,5-dithioacetic acid;(5-Carboxymethylsulfanyl-[1,3,4]thiadiazol-2-ylsulfanyl)-acetic acid
• CAS NO: 30843-69-7
• Molecular Formula: C₆H₆N₂O₄S₃
• Molecular Weight: 266.31784
• Mol File: 30843-69-7.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,3,4-Thiadiazole-2,5-dithioacetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,4-Thiadiazole-2,5-dithioacetic acid(30843-69-7)
• EPA Substance Registry System: 1,3,4-Thiadiazole-2,5-dithioacetic acid(30843-69-7)

Safety Data

• Hazardous Substances Data: 30843-69-7(Hazardous Substances Data)

Usage

Derivative of

Thiadiazole

Structural features

Two thioacetic acid groups attached to the nitrogen atoms

Potential applications

a. Pharmaceuticals
b. Agrochemicals

Biological properties

a. Antimicrobial activity
b. Antiparasitic activity

Unique molecular structure

Promising candidate for the development of new drugs and agrochemicals

Further research and development

May lead to the creation of novel and effective therapeutic agents and pesticides

Upstream product

• 53723-88-9 (5-thioxo-4,5-dihydro-[1,3,4]thiadiazol-2-ylmercapto)-acetic acid 
• 79-11-8 chloroacetic acid 
• 75646-23-0 2,2'-[1,3,4-thiadiazole-2,5-diylbis(thio)]diacetic acid dimethyl ester 
• 3926-62-3 sodium monochloroacetic acid 
• 1072-71-5 2,5-Dimercapto-1,3,4-thiadiazole 
• 1072-71-5 5-mercapto-1,3,4-thiadiazole-2(3H)-thione 
• 79-08-3 bromoacetic acid 

Downstream Products

• 1501966-51-3 [Zn(1,4-bis(imidazol-1-ylmethyl)benzene)(ADTZ)]·H₂O 
• 1501966-50-2 [Cd(1,4-bis(imidazol-1-ylmethyl)benzene)(ADTZ)(H₂O)] 

Relevant articles and documents

Triphenylphosphine-supported synthesis of two-dimensional silver(I) complex with (1,3,4-thiadiazole-2,5-diyldithio)diacetic acid

The reaction of dicarboxylate ligand, (1,3,4-thiadiazole-2,5-diyldithio)diacetic acid (H2tdza) with silver(I) acetate and triphenylphosphine (PPh3) facilitate the formation of complex [Ag2(tdza)(PPh3)2]n(1). The complex was characterized by elemental analysis, FT-IR spectroscopy,1H-NMR,13C-NMR and31P-NMR spectroscopy, and single crystal X-ray diffraction. Structural analysis revealed that complex 1 has a 2D topologically promising architecture as a result from the formation of 26-membered cyclic ring. The tdza2?ligand in 1 displays unprecedented μ4-bridging mode which is also the first example for this ligand. The interdigitating arrangement and π-π stacking between 2D arrays stabilized the formation of complex 1.

Application of 2,5-di(substituted formamyl methylthio group)-1,3,4-thiadiazole compound in inhibiting blue-green algae growth

The invention discloses application of a 2,5-di(substituted formamyl methylthio group)-1,3,4-thiadiazole compound in inhibiting blue-green algae growth, and belongs to the field of agricultural production and environmental protection. The structure of the 2,5-di(substituted formamyl methylthio group)-1,3,4-thiadiazole compound is as shown in a formula I, and R1, R2, R3, R4 and R5 in the formula I each adopt any one radical group of hydrogen or a halogen or an alkyl group or a hydroxyl group or trifluoromethyl or a nitro group. The compound has a good inhibiting effect on blue-green algae fructose-1,6-/sedoheptulose-1,7-biphosphatase; a good inhibiting effect on blue-green algae is achieved, and the compound can serve as the effective component of algicide to be applied to comprehensive treatment of blue-green algae bloom. The compound can be mixed with an allowable carrier in a water body or a diluent to be prepared into various commonly-used dosage forms such as a water mixture, an emulsion, an aqueous solution and a mobile agent to serve as the algicide for use. Please see the formula I in the description.