5448-29-3 Usage
Description
2-amino-1,1-dimethylethylisopropylamine, also known as a primary aliphatic amine, is a compound characterized by its unique structure. It is derived from propan-1,2-diamine, with an isopropyl group substitution at the N1 position and a methyl group at position 2. 2-amino-1,1-dimethylethylisopropylamine has been observed in cancer metabolism, making it a significant player in the field of medical research.
Uses
Used in Pharmaceutical Industry:
2-amino-1,1-dimethylethylisopropylamine is used as a metabolic marker for cancer detection due to its presence in cancer metabolism. Its identification in biological samples can aid in the early diagnosis and monitoring of various types of cancer, contributing to improved patient outcomes.
Used in Chemical Research:
As a unique amine compound, 2-amino-1,1-dimethylethylisopropylamine can be utilized in chemical research for the development of novel drugs and therapies. Its specific structural features may provide insights into the design of new molecules with potential applications in various medical and pharmaceutical contexts.
Used in Biochemical Studies:
2-amino-1,1-dimethylethylisopropylamine's presence in cancer metabolism makes it a valuable subject for biochemical studies. Researchers can investigate its role in the metabolic pathways of cancer cells, potentially leading to the discovery of new targets for cancer treatment and the development of more effective therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 5448-29-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,4 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5448-29:
(6*5)+(5*4)+(4*4)+(3*8)+(2*2)+(1*9)=103
103 % 10 = 3
So 5448-29-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H18N2/c1-6(2)9-5-7(3,4)8/h6,9H,5,8H2,1-4H3
5448-29-3Relevant articles and documents
Synthesis of 1,2-diamines, 2-imidazolidinones and 2-imidazolidinethiones from α-haloimines
De Kimpe,D'Hondt
, p. 1013 - 1017 (2007/10/02)
α-Bromo- and α-chloroaldimines 1 are easily converted into α-azidoaldimines 2 which are reduced by lithium aluminum hydride to afford N-monoalkylated 1,2-diamines 3. In a similar way, aromatic α-bromoketimines 7 are transformed into the corresponding α-azidoketimines 8 and α-monoalkylated l,2-diamines 9. The 1,2-diamines, thus obtained, are converted into 2-imidazolidinones 4, 10 and 2-imidazolidinethiones 5, 11.
