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6913-14-0

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6913-14-0 Usage

Description

3-Ethylsulfanyl-[1,2,4]thiadiazol-5-ylamine is a chemical compound that belongs to the thiadiazole group. It is a yellow crystalline solid with a molecular formula C5H8N4S2. 3-ETHYLSULFANYL-[1,2,4]THIADIAZOL-5-YLAMINE is known for its potential biological activity and is commonly used in the pharmaceutical industry.

Uses

Used in Pharmaceutical Industry:
3-Ethylsulfanyl-[1,2,4]thiadiazol-5-ylamine is used as an active pharmaceutical ingredient for its potential antibacterial properties, making it a candidate for the development of new antibiotics to combat resistant bacterial strains.
Used in Pharmaceutical Industry:
3-Ethylsulfanyl-[1,2,4]thiadiazol-5-ylamine is used as an antitumor agent due to its potential to inhibit the growth of cancer cells, offering a promising avenue for cancer treatment research.
Used in Pharmaceutical Industry:
3-Ethylsulfanyl-[1,2,4]thiadiazol-5-ylamine is used as an anti-inflammatory agent, leveraging its potential to reduce inflammation and alleviate symptoms associated with inflammatory conditions.
Used in Pharmaceutical Industry:
3-Ethylsulfanyl-[1,2,4]thiadiazol-5-ylamine is used as an antiviral agent, with research exploring its potential to inhibit viral replication and treat viral infections.
Its unique chemical structure and potential applications make 3-Ethylsulfanyl-[1,2,4]thiadiazol-5-ylamine a promising candidate for further research and development in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 6913-14-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,1 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6913-14:
(6*6)+(5*9)+(4*1)+(3*3)+(2*1)+(1*4)=100
100 % 10 = 0
So 6913-14-0 is a valid CAS Registry Number.
InChI:InChI=1/C4H7N3S2/c1-2-8-4-6-3(5)9-7-4/h2H2,1H3,(H2,5,6,7)

6913-14-0Downstream Products

6913-14-0Relevant articles and documents

Oxidative cyclization of dithiobiuret under basic conditions and theoretical tautomeric studies of 5-amino-2,3-dihydro-1,2,4-thiadiazole-3-thione

Cho, Nam Sook,Kim, Young Hoon,Park, Mi Sun,Kim, Eun Hee,Kang, Sung Kwon,Park, Chang-Moon

, p. 1401 - 1409 (2007/10/03)

The oxidative cyclization of dithiobiuret under basic conditions (NaOH-H2O2 or CH3CO3H) afforded bis(5-amino-1,2,4-thiadiazolyl) 3,3′-disulfide (5), oxidative dimer form of 5-amino-3-mercapto-1,2,4-thiadiazole (

Nitrogen and/or sulfur containing heterocyclic azo dyes with aniline, tetrahydroquinoline and benzomorpholine couplers having sulfate group

-

, (2008/06/13)

Disclosed are azo dyes prepared by diazotizing heterocyclic amines such as 2-aminobenzothiazole, 3-amino-2,1-benzisothiazole, 5-amino-1,2,4-thiadiazole, 5-aminoisothiazole, 5-aminopyrazole, 2-aminothiophene and 2-amino-1,3,4-thiadiazole, followed by coupling with certain aniline, tetrahydroquinoline, or benzomorpholine compounds containing sulfate groups. These amines may be substituted with a large variety of groups including lower alkyl, lower alkoxy, cyano, carbamoyl, sulfamoyl, and halogen. These dyes have excellent dyeing properties on polyamide fibers and also impart color to cellulose acetate fibers and wool.

Azo dyes from five membered ring heterocyclic amines and aniline, tetrahydroquinoline and benzomorpholine couplers containing thiosulfate alkyl groups

-

, (2008/06/13)

Disclosed are mono azo dyes derived from diazotized 5-membered heterocyclic amines and certain aniline, 1,2,3,4-tetrahydroquinoline, and benzomorpholine couplers containing thiosulfate alkyl groups. These dyes are useful for dyeing synthetic fibers, cellulose acetate and wool, and particularly impart fast violet to blue shades on polyamide fibers, and in general, exhibit improved properties such as fastness to light, sublimation, ozone, oxides of nitrogen, perspiration, crock, and wash, and exhibit excellent build, pH stability, bloom resistance, depth of shade, leveling, migration, and the like. The dyes have the general formula: wherein D is a thiadiazol, isothiazol, pyrazol or thiophene type radical, and the Coupler is an aniline, tetrahydroquinoline, or benzomorpholine derivative wherein a --ZSSO3 M group is attached to the nitrogen thereof, the coupler ring may contain substituents such as alkyl, alkoxy, halogen, acylamido, alkylthio or aryloxy, the remaining hydrogen of the aniline coupler may be replaced by a substituent such as alkyl, substituted alkyl, alkenyl, aryl, or cycloalkyl, M is Na+, K+, NH4+ or H+, and Z is a linking group such as ethylene.

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