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1,2,5-Thiadiazole-3,4-dicarboxylicacid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

3762-94-5

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3762-94-5 Usage

Type of compound

Heterocyclic organic compound

Structure

Contains both sulfur and nitrogen atoms

Common use

Building block in the synthesis of pharmaceuticals and agrochemicals

Functional groups

Carboxylic acid groups

Versatility

Can form coordination complexes with metal ions

Applications

Useful in various industrial and research applications

Biological activities

Being studied for potential medicinal properties

Check Digit Verification of cas no

The CAS Registry Mumber 3762-94-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,6 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3762-94:
(6*3)+(5*7)+(4*6)+(3*2)+(2*9)+(1*4)=105
105 % 10 = 5
So 3762-94-5 is a valid CAS Registry Number.
InChI:InChI=1/C4H2N2O4S/c7-3(8)1-2(4(9)10)6-11-5-1/h(H,7,8)(H,9,10)

3762-94-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,5-thiadiazole-3,4-dicarboxylic acid

1.2 Other means of identification

Product number -
Other names 1,2,5-Thiadiazole-3,4-dicarboxylicacid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3762-94-5 SDS

3762-94-5Relevant academic research and scientific papers

Method for preparing 1,2,3-thiadiazole-4-carboxylic acid

-

Paragraph 0019; 0023; 0024; 0025, (2017/04/22)

The invention relates to a method for preparing 1,2,3-thiadiazole-4-carboxylic acid, which comprises: preparing 4,5-dicyano-1,2,3-thiadiazole by reaction between diaminomaleonitrile and dichloroethane; preparing 1,2,3-thiadiazole 4,5-dicarboxylic acid by the cyan-hydrolysis of 4,5-dicyano-1,2,3-thiadiazole; and preparing 1,2,3-thiadiazole-4-carboxylic acid by the decarboxylation reaction of 1,2,3-thiadiazole 4,5-dicarboxylic acid. The provided process route is high in synthesis rate of the target product, moreover, the process route can be magnified, the raw materials can be easily obtained and are cheap, and industrial production can be carried out.

Topological modulation of metal-thiadiazole dicarboxylate coordination polymers through auxiliary ligand alteration

Zhao, Zhen-Xin,Li, Yun-Wu,Liu, Sui-Jun,Wang, Li-Fu,Chang, Ze,Xu, Jian,Zhang, Ying-Hui

, p. 4301 - 4308 (2015/06/16)

Five new CoII/ZnII coordination polymers (CPs), namely [Co(tdzdc)(4,4′-bipy)(H2O)]n (1), {[Co(tdzdc)(bpp)(H2O)]·3H2O}n (2), {[Zn2(tdzdc)2(4,4′-bipy)(H2O)2]·3H2O}n (3), [Zn2(tdzdc)2(obpy)(H2O)2]n (4) and [Zn(tdzdc)(tmb)]n (5), have been synthesized based on the primary ligand 1,2,5-thiadiazole-3,4-dicarboxylic acid (H2tdzdc) together with four selected N/O-donor auxiliary ligands, i.e., 4,4′-bipy: 4,4′-bipyridine, bpp: 1,3-bi(pyridin-4-yl)propane, obpy: [4,4′-bipyridine]-N,N′-dioxide, and tmb: 1,4-bis((1H-1,2,4-triazol-1-yl)methyl)benzene. Single-crystal structural analyses unveil different topologies and interpenetration degrees of 1-5, associated with four different kinds of coordination modes of H2tdzdc that depend on the auxiliary ligands used. CPs 1-4 are all constructed by extending the one-dimensional metal-ligand chain through the respective auxiliary ligands. Among them, the linear rigid auxiliary ligands (i.e., bipy and obpy) generate two-dimensional planes of 1, 3 and 4, which exhibit different interpenetration degrees of 0, 2 and 3, respectively, while the flexible bpp auxiliary ligand forms a three-dimensional net of 2. In contrast, CP 5 has a basic structural unit comprising dinuclear metal clusters that facilitate the formation of a 3-fold interpenetrated two-dimensional net extended through the tmb auxiliary ligand. Furthermore, magnetic investigations of the two CoII-based CPs reveal that despite being mediated by syn-anti bridging of the carboxylate, both 1 and 2 display antiferromagnetic and canted antiferromagnetic behaviors, respectively.

Organic Heterocyclothiazenes. Part 5. Cycloaddition Reactions of Tetrasulphur Tetranitride with Highly Electron Deficient Alkynes

Dunn, Peter J.,Rees, Charles W.

, p. 1579 - 1584 (2007/10/02)

In contrast with previous, complex, S4N4-alkyne reactions, treatment of butynedinitrile and S4N4 is found to give 1,3,5,2,4-trithiadiazepine-6,7-dicarbonitrile (8) and 1,2,5-thiadiazole-3,4-dicarbonitrile (9) very cleanly and in high yield.Hexafluorobut-2

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