313469-03-3 Usage
Uses
Used in Organic Chemistry:
10-N-Boc-amino-dec-1-ene is used as a synthetic intermediate for the preparation of various organic compounds. Its Boc-protected amino group allows for selective reactions at other sites on the molecule, facilitating the synthesis of complex organic structures.
Used in Pharmaceutical Industry:
10-N-Boc-amino-dec-1-ene is used as a building block in the development of pharmaceutical compounds. Its unique structure can be incorporated into drug molecules to impart specific biological activities or improve pharmacokinetic properties, such as solubility, stability, or bioavailability.
Used in Materials Science:
10-N-Boc-amino-dec-1-ene is used as a precursor for the synthesis of novel materials with tailored properties. Its incorporation into polymers, for example, can result in materials with enhanced mechanical strength, thermal stability, or specific chemical functionalities.
Used in Peptide Synthesis:
10-N-Boc-amino-dec-1-ene is used as a protected amino acid in the synthesis of peptides and proteins. The Boc group allows for the stepwise assembly of peptide chains, protecting the amino group from unwanted side reactions until the desired sequence is achieved.
Used in Catalyst Design:
10-N-Boc-amino-dec-1-ene can be used as a ligand or a component in the design of catalysts for various chemical reactions. Its unique structure may impart specific binding properties or electronic effects that enhance the catalytic activity or selectivity of the resulting catalyst.
Used in Bioconjugation:
10-N-Boc-amino-dec-1-ene can be used as a linker in bioconjugation processes, connecting biological molecules such as proteins, nucleic acids, or carbohydrates to other molecules or surfaces. The Boc-protected amino group can be selectively deprotected and reacted with target molecules, facilitating the formation of stable conjugates.
Used in Drug Delivery Systems:
10-N-Boc-amino-dec-1-ene can be incorporated into drug delivery systems to improve the solubility, stability, or targeted delivery of therapeutic agents. Its unique structure may allow for the development of novel drug carriers or the modification of existing systems to enhance their performance.
Used in Chemical Sensors:
10-N-Boc-amino-dec-1-ene can be used as a component in the design of chemical sensors, exploiting its unique chemical reactivity or binding properties to detect specific analytes or environmental conditions.
Used in Surface Modification:
10-N-Boc-amino-dec-1-ene can be used to modify the surface properties of various materials, such as metals, polymers, or nanoparticles. Its incorporation can result in surfaces with enhanced properties, such as improved biocompatibility, wettability, or chemical resistance.
Used in Supramolecular Chemistry:
10-N-Boc-amino-dec-1-ene can be used as a building block in supramolecular chemistry, participating in non-covalent interactions such as hydrogen bonding, π-π stacking, or metal coordination. This can lead to the formation of complex supramolecular assemblies with unique properties or functions.
Check Digit Verification of cas no
The CAS Registry Mumber 313469-03-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,3,4,6 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 313469-03:
(8*3)+(7*1)+(6*3)+(5*4)+(4*6)+(3*9)+(2*0)+(1*3)=123
123 % 10 = 3
So 313469-03-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H29NO2/c1-5-6-7-8-9-10-11-12-13-16-14(17)18-15(2,3)4/h5H,1,6-13H2,2-4H3,(H,16,17)
313469-03-3Relevant academic research and scientific papers
Yun, Hwayoung,Sim, Jaehoon,An, Hongchan,Lee, Jeeyeon,Lee, Hun Seok,Shin, Young Kee,Paek, Seung-Mann,Suh, Young-Ger
, p. 7127 - 7135 (2014)
The rational design and synthesis of a biochemical probe of natural (+)-macrosphelide A, a potent cell-cell adhesion inhibitor, was completed to aid in the identification of its biological target. The key features of the synthesis include: (1) an efficient synthesis of the macrosphelide core structure using Yamaguchi-Hirao alkynylation, (2) a cross metathesis to connect a linker unit to the allyl-macrosphelide and (3) coupling of the linker-bound macrosphelide A with a chemical biotin tag. This journal is the Partner Organisations 2014.
Decarbonylative approach to the synthesis of enamides from amino acids: Stereoselective synthesis of the (Z)-aminovinyl-d-cysteine unit of mersacidin
Garcia-Reynaga, Pablo,Carrillo, Angela K.,Vannieuwenhze, Michael S.
, p. 1030 - 1033 (2012/04/04)
The Pd- and Ni-promoted decarbonylation of amino acid thioesters proceeds smoothly to yield enamides. The synthesis of the (S)-(Z)-AviMeCys subunit of mersacidin, an MRSA-active lantibiotic, via this approach, is described.
