73696-35-2 Usage
Uses
Used in Pharmaceutical Research:
5,6,7,8-Tetrahydro-2-phenyl-4H-[1]benzothieno[2,3-d][1,3]oxazin-4-one is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and reactivity make it a promising candidate for the development of new drugs with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, 5,6,7,8-Tetrahydro-2-phenyl-4H-[1]benzothieno[2,3-d][1,3]oxazin-4-one is utilized as a versatile building block for the creation of a wide range of organic compounds. Its ability to participate in various chemical reactions allows for the synthesis of complex molecules with diverse properties and potential applications.
Used in Medicinal Chemistry:
5,6,7,8-Tetrahydro-2-phenyl-4H-[1]benzothieno[2,3-d][1,3]oxazin-4-one plays a significant role in medicinal chemistry, where it is employed as a structural component in the design and development of new drugs. Its unique features contribute to the discovery of compounds with improved pharmacological properties and therapeutic potential.
Used in Drug Discovery:
As a valuable tool in drug discovery efforts, 5,6,7,8-Tetrahydro-2-phenyl-4H-[1]benzothieno[2,3-d][1,3]oxazin-4-one aids researchers in identifying and optimizing novel compounds with potential biological activity. Its presence in a compound can influence its pharmacokinetic and pharmacodynamic properties, making it an important factor in the development of effective therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 73696-35-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,6,9 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 73696-35:
(7*7)+(6*3)+(5*6)+(4*9)+(3*6)+(2*3)+(1*5)=162
162 % 10 = 2
So 73696-35-2 is a valid CAS Registry Number.
73696-35-2Relevant academic research and scientific papers
Synthesis of some new tetrahydrobenzo[b] thiophene derivatives and tetrahydrobenzo-thienopyrimidine derivatives under microwave irradiation
Abdalha,El-Kassaby, M.K. Abou,El-Regal,Ali
, p. 2811 - 2821 (2011/09/12)
2-Phenyl-5,6,7,8-tetrahydro-4H-benzothieno[2,3-d][1,3]oxazin-4-one (4) was reacted with either aliphatic or aromatic primary amines such as benzylamine, cyclohexylamine, p-toluidine, and=or p-anisidine to give carboxamide derivatives 5a-d, respectively. A
A new, general approach for the synthesis of heteroannulated 3,1-oxazin-4-ones
Wamhoff,Herrmann,Stolben,Nieger
, p. 581 - 594 (2007/10/02)
β-(N-Triphenylphosphoranyliden)-enamino esters afford the synthetically useful heteroannulated 3,1-oxazin-4-ones with aroyl chlorides in different solvents. The reaction proceeds in one step and in high yields and appears to be independent of the reactivity of the heterocyclic substrate.
Heterocyclic β-Enamino Esters, 27. Synthesis of Heterocondensed 6H-1,3-Oxazin-6-ones from N-Acylenamino Esters in the System Triphenylphosphane/Hexachloroethane/Triethylamine
Achakzi, Darwizah,Ertas, Muemtaz,Appel, Rolf,Wamhoff, Heinrich
, p. 3188 - 3194 (2007/10/02)
A simple ring closure reaction of N-acylenamino esters (1b, e, 2, 3a - f, 7) in the system triphenylphosphane/hexachloroethane/triethylamine is described proceeding with high yields.Under chlorinating 3-ester cleavage heterocondensed 6H-1,3-oxazin-6-ones
FUNCTIONAL DERIVATIVES OF THIOPHENE. 18. SYNTHESIS OF 4-OXOTHIENOOXAZINE DERIVATIVES AND THIOPHENE-3-CARBOXYLIC ACID HYDRAZIDES
Kharizomenova, I.A.,Samsonova, N.V.,Kaplina, N.V.,Kapustina, M.V.,Grinev, A.N.
, p. 36 - 37 (2007/10/02)
2-Aryl-4-oxothienooxazine derivatives were synthesized.Opening of the oxazine ring to give 2-benzamidothiophene-3-carboxylic acid hydrazide derivatives is observed when these compounds are treated with hydrazine hydrate.
