5554-48-3 Usage
Uses
Used in Pharmaceutical Research and Development:
1,3-Thiazidine-2-thione is utilized as a key intermediate in the synthesis of various bioactive compounds and pharmaceutical drugs. Its unique structure allows it to serve as a valuable building block in the development of new chemical entities for medicinal applications.
Used in Organic Synthesis:
In the field of organic synthesis, 1,3-Thiazidine-2-thione is employed for its versatile chemical properties, which make it a useful component in creating a range of chemical compounds.
Used in Anticancer Applications:
1,3-Thiazidine-2-thione has been studied for its potential as an anti-cancer agent, indicating its use in developing treatments that could target cancer cells.
Used in Anti-inflammatory Applications:
1,3-Thiazidine-2-thione is also recognized for its potential anti-inflammatory properties, suggesting a use in the creation of medications aimed at reducing inflammation.
Used in Anti-bacterial Applications:
Furthermore, 1,3-Thiazidine-2-thione has shown potential anti-bacterial activities, which implies its use in the development of antibiotics or other treatments to combat bacterial infections.
Used in Agricultural Applications:
Given its potential as a building block for new chemical entities, 1,3-Thiazidine-2-thione may also find use in the agricultural sector, possibly in the development of pesticides or other agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 5554-48-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,5 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5554-48:
(6*5)+(5*5)+(4*5)+(3*4)+(2*4)+(1*8)=103
103 % 10 = 3
So 5554-48-3 is a valid CAS Registry Number.
InChI:InChI=1/C4H7NS2/c6-4-5-2-1-3-7-4/h1-3H2,(H,5,6)
5554-48-3Relevant academic research and scientific papers
Photochemical Reactions of N-Acyldithiocarbamates and N-Acylthiocarbamates
Sakamoto, Masami,Watanbe, Shoji,Fujita, Tsutomu,Aoyama, Hiromu,Omote, Yoshimori
, p. 2541 - 2546 (2007/10/02)
Photochemical hydrogen abstraction from N-acyltetrahydro-1,3-thiazine-2-thiones, N-acyloxazolidine-2-thiones and N-acyltetrahydro-1,3-oxazine-2-thiones have been studied.Irradiation of N-(diphenylacetyl)- and N-(alkoxyacetyl)tetrahydro-1,3-thiazine-2-thio
PHOTOCHEMICAL REACTIONS OF 3-ACYL-2-THIOTETRAHYDRO-1,3-THIAZINES; A NEW SYNTHESIS OF CEPHAM ANALOGUES
Sakamoto, Masami,Aoyama, Hiromu,Omote, Yoshimori
, p. 1335 - 1338 (2007/10/02)
Photolysis of 3-acyl-2-thiotetrahydro-1,3-thiazines followed by acetylation gave bicyclic β-lactams accompanied by Type II cleavage products.High temperature photolysis of them gave 2,9-dithia-6-azabicyclo(4,3,0)nonan-7-ones involving α-cleavage reactions
On 1,3-Thiazines, XX: Transacylating N-Acyltetrahydro-1,3-thiazine-2-thiones
Hanefeld, Wolfgang,Bercin, Erdogan
, p. 74 - 79 (2007/10/02)
The synthesis of novel N-acyltetrahydro-1,3-thiazine-2-thiones 3 with transacylating activity towards nucleophilic compounds is described.
