216961-61-4 Usage
Description
1-BOC-1,10-DIAMINODECANE, also known as tert-Butyl (10-aminodecyl)carbamate, is a chemical compound featuring an alkane chain with terminal amine and Boc-protected amino groups. 1-BOC-1,10-DIAMINODECANE is characterized by its reactivity with various functional groups, such as carboxylic acids, activated NHS esters, and carbonyls (ketone, aldehyde). The Boc group present in the molecule can be deprotected under mild acidic conditions, resulting in the formation of a free amine.
Uses
Used in Chemical Synthesis:
1-BOC-1,10-DIAMINODECANE is used as a building block in the synthesis of various chemical compounds due to its reactive amine groups and Boc-protected nature. The ability to form covalent bonds with different functional groups makes it a versatile component in creating a wide range of molecules.
Used in PROTAC Linker Synthesis:
1-BOC-1,10-DIAMINODECANE is used as a PROTAC linker in the synthesis of proteolysis-targeting chimeras (PROTACs). Its terminal amine and Boc-protected amino groups facilitate the formation of stable and specific linkages with target proteins, enabling the development of novel protein degradation therapies.
Used in Conjugation Applications:
1-BOC-1,10-DIAMINODECANE is utilized in conjugation applications, where its reactive amine groups allow for the attachment of various molecules, such as drugs, dyes, or other targeting agents, to form conjugates with specific functionalities.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1-BOC-1,10-DIAMINODECANE is used as a key intermediate in the development of new drugs and drug delivery systems. Its ability to form stable linkages with target molecules makes it a valuable component in the design and synthesis of innovative therapeutic agents.
Used in Research and Development:
1-BOC-1,10-DIAMINODECANE is employed as a research tool in the field of chemical biology and medicinal chemistry. Its unique properties and reactivity enable scientists to explore new chemical reactions, develop novel synthetic strategies, and create new compounds with potential applications in various fields, including drug discovery and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 216961-61-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,6,9,6 and 1 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 216961-61:
(8*2)+(7*1)+(6*6)+(5*9)+(4*6)+(3*1)+(2*6)+(1*1)=144
144 % 10 = 4
So 216961-61-4 is a valid CAS Registry Number.
InChI:InChI=1/C15H32N2O2/c1-15(2,3)19-14(18)17-13-11-9-7-5-4-6-8-10-12-16/h4-13,16H2,1-3H3,(H,17,18)
