133891-60-8 Usage
Type of compound
Azetidine
Azetidine is a cyclic amine containing four carbon atoms.
Structure
Diphenylmethyl group attached to the nitrogen atom
The diphenylmethyl group consists of a carbon atom bonded to two phenyl groups (C6H5), which is attached to the nitrogen atom in the azetidinamine ring.
Structure
Two methyl groups on the azetidinamine ring
The azetidinamine ring has two methyl groups (CH3) attached to it, which are located at the 3rd and 1st positions.
Application
Building block in organic synthesis
This compound is used as a starting material or intermediate in the synthesis of more complex organic molecules.
Application
Pharmaceutical research
It is used in the development of new drugs or active pharmaceutical ingredients.
Potential applications
Development of new drugs
The compound may have potential applications in the development of new drugs due to its unique structure and reactivity.
Specific properties
Varies based on application and intended use
The precise properties, functions, and uses of this compound may vary depending on the specific application and intended use in the field of organic synthesis or pharmaceutical research.
Check Digit Verification of cas no
The CAS Registry Mumber 133891-60-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,8,9 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 133891-60:
(8*1)+(7*3)+(6*3)+(5*8)+(4*9)+(3*1)+(2*6)+(1*0)=138
138 % 10 = 8
So 133891-60-8 is a valid CAS Registry Number.
133891-60-8Relevant articles and documents
7-Azetidinylquinolones as antibacterial agents. Synthesis and structure- activity relationships
Frigola,Pares,Corbera,Vano,Merce,Torrens,Mas,Valenti
, p. 801 - 810 (2007/10/02)
A series of novel antibacterial quinolones and naphthyridones has been prepared which contain 7-azetidinyl substituents in place of the usual piperazine or aminopyrrolidine groups. These azetidinyl derivatives were evaluated for in vitro activity by deter
