199273-16-0 Usage
Uses
Used in Pharmaceutical Industry:
N-BOC-2-AMINO-5-BROMOBENZALDEHYDE is utilized as a key building block in the synthesis of various pharmaceutical compounds. Its Boc-protected amine group allows for the controlled introduction of amino functionalities into complex organic molecules, while the bromine substituent can be employed for further diversification of the molecular structure, enhancing the drug's therapeutic potential.
Used in Agrochemical Industry:
In the agrochemical sector, N-BOC-2-AMINO-5-BROMOBENZALDEHYDE serves as an essential intermediate for the development of novel agrochemicals. Its reactivity and functional groups enable the creation of molecules with specific pesticidal or herbicidal properties, contributing to the advancement of crop protection strategies.
Used in Organic Synthesis Research:
N-BOC-2-AMINO-5-BROMOBENZALDEHYDE is employed as a model compound in organic synthesis research. Its unique structure and reactivity make it an ideal candidate for studying various chemical reactions and mechanisms, providing insights into the development of new synthetic methodologies and the understanding of reaction pathways.
Used in Chemical Education:
N-BOC-2-AMINO-5-BROMOBENZALDEHYDE is also used in chemical education to illustrate the principles of organic synthesis, protection strategies, and functional group manipulation. It serves as a practical example for teaching students about the importance of intermediates in organic chemistry and the strategies employed to construct complex molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 199273-16-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,2,7 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 199273-16:
(8*1)+(7*9)+(6*9)+(5*2)+(4*7)+(3*3)+(2*1)+(1*6)=180
180 % 10 = 0
So 199273-16-0 is a valid CAS Registry Number.
199273-16-0Relevant academic research and scientific papers
Organometallic ligands for the localization and quantification of amyloid in vivo and in vitro
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, (2008/06/13)
Novel organometallic compounds for binding amyloid are described. Methods using such compounds for determining by imaging the localization or quantification of amyloid fibrils in a mammal, for diagnosing the degree of progression of Alzheimer's disease in a mammal, for monitoring the response to a therapy in a mammal having Alzheimer's disease, for identifying an agent useful for treating Alzheimer's disease, for treating Alzheimer's disease, and for detecting the presence of the infectious form of the prion protein, are also described.
