109768-66-3 Usage
Description
(4H-BENZO[D][1,3]THIAZIN-2-YL)-PHENYL-AMINE is a chemical compound characterized by its molecular formula C13H10N2S. It is a member of the thiazine class of compounds, which are known for their seven-membered heterocyclic ring containing sulfur and nitrogen atoms. This particular compound features a thiazine ring connected to a phenyl group and an amine functional group, making it a versatile building block in organic synthesis and medicinal chemistry. Its unique structure and properties render it a valuable asset for researchers in the fields of drug development and chemical synthesis.
Uses
Used in Pharmaceutical Industry:
(4H-BENZO[D][1,3]THIAZIN-2-YL)-PHENYL-AMINE is used as a building block for the synthesis of various pharmaceuticals and bioactive compounds. Its unique structure allows for the creation of a wide range of molecules with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, (4H-BENZO[D][1,3]THIAZIN-2-YL)-PHENYL-AMINE serves as a key intermediate for the preparation of complex organic molecules. Its thiazine ring and phenyl group provide a foundation for further chemical modifications, enabling the development of novel compounds with diverse properties and applications.
Used in Medicinal Chemistry:
(4H-BENZO[D][1,3]THIAZIN-2-YL)-PHENYL-AMINE is utilized in medicinal chemistry as a starting point for the design and development of new drugs. Its structural features can be exploited to target specific biological pathways or receptors, potentially leading to the discovery of innovative treatments for various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 109768-66-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,7,6 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 109768-66:
(8*1)+(7*0)+(6*9)+(5*7)+(4*6)+(3*8)+(2*6)+(1*6)=163
163 % 10 = 3
So 109768-66-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H12N2S/c1-2-7-12(8-3-1)15-14-16-13-9-5-4-6-11(13)10-17-14/h1-9H,10H2,(H,15,16)
109768-66-3Relevant articles and documents
P(III)-Mediated Cascade C-N/C-S Bond Formation: A Protocol towards the Synthesis of N,S-Heterocycles and Spiro Compounds
Polina, Saibabu,Putta, V. P. Rama Kishore,Gujjarappa, Raghuram,Singh, Virender,Pujar, Prasad Pralhad,Malakar, Chandi C.
, p. 431 - 445 (2020/12/07)
A P(III)-mediated entry towards construction of C?N/C?S bond has been devised. The developed heterocyclization method was exercised for the synthesis of a diverse range of N,S-heterocycles and related spiro molecules. P(NMe2)3 revealed the maximum efficacies under the aerobic reaction conditions and a spectrum of bis-nucleophiles, and isothiocyanates were tolerated well to serve the access of manifold immense molecules. (Figure presented.).
A Bench-Stable Vilsmeier Reagent for in situ Alcohol Activation: Synthetic Application in the Synthesis of 2-Amino-2-Thiazolines
Corbett, Michael T.,Caille, Seb
, p. 2845 - 2850 (2017/10/06)
A robust, chemoselective direct condensation/cyclization of thioureas and amino alcohols is described. Employing a bench-stable Vilsmeier reagent, methoxymethylene- N, N -dimethyliminium methyl sulfate, the selective in situ activation of alcohols is achieved with high efficiency and broad functional-group tolerance. The reversible interaction of the Vilsmeier reagent with substrate was key to the success of this activation strategy.
