5368-66-1 Usage
Description
1,2,4,5-Tetrahydrobenzo[d]oxepine, also known as tetrahydrobenzoxepine or oxepine, is a heterocyclic compound with a molecular formula C9H9NO. It is a bicyclic molecule consisting of a six-membered benzene ring fused to a seven-membered oxygen-containing oxepine ring. This chemical compound has a variety of industrial and pharmaceutical uses due to its unique structure and properties.
Used in Pharmaceutical Industry:
1,2,4,5-Tetrahydrobenzo[d]oxepine is used as a building block for the synthesis of pharmaceutical drugs. Its unique structure allows it to be incorporated into various drug molecules, potentially leading to the development of new and improved medications.
Used in Agrochemical Industry:
1,2,4,5-Tetrahydrobenzo[d]oxepine is used as a building block in the synthesis of agrochemicals. Its incorporation into agrochemical compounds can contribute to the development of more effective and targeted pest control solutions.
Used in Organic Chemistry:
1,2,4,5-Tetrahydrobenzo[d]oxepine is used as a reagent in organic chemistry reactions. Its unique structure and properties make it a valuable component in various chemical processes, potentially leading to the creation of new and innovative organic compounds.
Used in Material Science:
1,2,4,5-Tetrahydrobenzo[d]oxepine has applications in the development of new materials. Its unique structure and properties can be utilized to create novel materials with specific characteristics, potentially leading to advancements in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 5368-66-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,6 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5368-66:
(6*5)+(5*3)+(4*6)+(3*8)+(2*6)+(1*6)=111
111 % 10 = 1
So 5368-66-1 is a valid CAS Registry Number.
5368-66-1Relevant articles and documents
Synthesis of 3-substituted tetrahydrofuran and 4-substituted tetrahydropyran derivatives by cyclization of dicarboxylic acids with InBr 3/TMDS
Pehlivan, Leyla,Metay, Estelle,Delbrayelle, Dominique,Mignani, Gerard,Lemaire, Marc
supporting information; experimental part, p. 4689 - 4693 (2012/09/22)
An efficient reduction followed by cyclization of diacid compounds with the InBr3/TMDS system is reported. This system allows the formation of five- and six-membered ring ethers substituted in the 3- or 4-position. Copyright
