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Trans-3-cyano-1-(diphenylmethyl)-2-methylazetidine is a complex chemical compound characterized by its trans isomer configuration, where the two bulky diphenylmethyl groups are positioned in opposite directions. trans-3-cyano-1-(diphenylmethyl)-2-methylazetidine features a cyano group, a diphenylmethyl group, and a methylazetidine ring, which collectively contribute to its unique structure and multiple functional groups. The presence of these functional groups suggests potential applications in organic synthesis and the pharmaceutical industry, making it a valuable building block for developing new molecules with diverse properties and potential biological activities.

159556-79-3

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159556-79-3 Usage

Uses

Used in Organic Synthesis:
Trans-3-cyano-1-(diphenylmethyl)-2-methylazetidine is used as a building block in organic synthesis for its unique structure and multiple functional groups. The cyano group, in particular, can be utilized in various synthetic reactions, such as nucleophilic addition, to form new compounds with different functional groups and properties.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, trans-3-cyano-1-(diphenylmethyl)-2-methylazetidine is used as a starting material or intermediate in the synthesis of various drug candidates. Its unique structure and functional groups can be exploited to design and develop new molecules with potential therapeutic applications. trans-3-cyano-1-(diphenylmethyl)-2-methylazetidine's versatility in organic synthesis allows for the creation of diverse drug candidates with improved pharmacological properties, such as increased potency, selectivity, and bioavailability.
Used in Medicinal Chemistry Research:
Trans-3-cyano-1-(diphenylmethyl)-2-methylazetidine is also used in medicinal chemistry research as a tool to explore the structure-activity relationships (SAR) of various biologically active molecules. By incorporating trans-3-cyano-1-(diphenylmethyl)-2-methylazetidine into different molecular frameworks, researchers can gain insights into the role of its functional groups in modulating the biological activity of the resulting compounds. This information can be valuable in the design of more effective and selective drug candidates targeting specific therapeutic areas.

Check Digit Verification of cas no

The CAS Registry Mumber 159556-79-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,5,5 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 159556-79:
(8*1)+(7*5)+(6*9)+(5*5)+(4*5)+(3*6)+(2*7)+(1*9)=183
183 % 10 = 3
So 159556-79-3 is a valid CAS Registry Number.

159556-79-3Downstream Products

159556-79-3Relevant academic research and scientific papers

7-Azetidinylquinolones as antibacterial agents. 2. Synthesis and biological activity of 7-(2,3-disubstituted-1-azetidinyl)-4-oxoquinoline- and -1,8-naphthyridine-3-carboxylic acids. Properties and structure-activity relationships of quinolones with an aze

Frigola,Torrens,Castrillo,Mas,Vano,Berrocal,Calvet,Salgado,Redondo,Garcia-Granda,Valenti,Quintana

, p. 4195 - 4210 (1994)

A series of 7-(2,3-disubstituted-1-azetidinyl)-1,4-dihydro-6-fluoro-4- oxoquinoline- and -1,8-naphthyridine-3-carboxylic acids, with varied substituents at the 1-, 5-, and 8-positions, was prepared to study the effects on potency and physicochemical prope

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