54262-75-8 Usage
Description
1-Azetidinepropanamine, also known as N-Azetidine-3-propanamine or 1-Amino-3-azetidinepropane, is a cyclic amine with the molecular formula C5H11N. It features a four-membered ring containing one nitrogen atom and is commonly used as a building block in organic synthesis and pharmaceutical research.
Uses
Used in Pharmaceutical Research:
1-Azetidinepropanamine is used as a key intermediate for the synthesis of various pharmaceutical drugs, particularly for the development of antiviral and anticancer agents. Its unique cyclic structure and amine functionality make it a valuable component in the creation of new therapeutic compounds.
Used in Organic Synthesis:
1-Azetidinepropanamine is used as a building block in organic synthesis, allowing for the construction of complex organic molecules. Its reactivity and structural properties contribute to the synthesis of a wide range of organic compounds.
Used in Academic and Industrial Research:
Due to its limited commercial availability, 1-Azetidinepropanamine is primarily used in academic and industrial research settings. It serves as a reagent in various organic chemistry reactions and is studied for its potential use in the development of new materials.
Check Digit Verification of cas no
The CAS Registry Mumber 54262-75-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,2,6 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 54262-75:
(7*5)+(6*4)+(5*2)+(4*6)+(3*2)+(2*7)+(1*5)=118
118 % 10 = 8
So 54262-75-8 is a valid CAS Registry Number.
54262-75-8Relevant articles and documents
KINETICS AND MECHANISM OF CHLOROPROPYLAMINE CYCLIZATIONS
Chernitskii, K. V.,Bobylev, V. A.,Veselkov, N. Yu.
, p. 546 - 551 (2007/10/02)
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CATALYTIC ALKYL GROUP EXCHANGE REACTION OF PRIMARY AND SECONDARY AMINES.
Murahashi,Yoshimura,Tsumiyama,Kojima
, p. 5002 - 5011 (2007/10/02)
It has been shown that primary and secondary amines undergo alkyl group exchange reactions upon treatment with palladium catalyst as depicted in an operationally simple and efficient reaction which provides a convenient method for synthesis of unsymmetrical amines. The application of the reaction for the preparation of various substituted amines and heterocyclic compounds such as hexahydropyrimidine tetrahydropyrimidine, imidazolidine, and imidazoles is described. The preparation of polyamines such as H//2N(CH//2)//mNH(CH//2)//nNH//2 (10) and H//2N(CH//2)//lNH(CH//2)//mNH(CH//2)//nNH//2 (l-n, equals 2,3; 11) is readily performed by the appadium-catalyzed reactions of azetidine (6) and aziridine (7) via azetine (9) and azirine intermediates. The mechanism the palladium-catalyzed reaction has been extensively studied on the carbonylation, racemization, and deuteurium-exchange reaction of (S)-( minus )- alpha -phenylethylamine (17).