56877-44-2 Usage
Uses
Used in Organic Synthesis:
γ-Carboxyglutamic Acid γ,γ-Di-t-butyl Ester is used as an intermediate in the synthesis of various organic compounds. Its unique structure and reactivity make it a valuable building block for creating complex molecules with specific properties and functions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, γ-Carboxyglutamic Acid γ,γ-Di-t-butyl Ester is used as a precursor for the development of new drugs. Its ability to form stable esters and its compatibility with various chemical reactions make it a promising candidate for designing innovative therapeutic agents.
Used in Chemical Research:
γ-Carboxyglutamic Acid γ,γ-Di-t-butyl Ester is also employed in chemical research to study the properties and behavior of carboxylic acid esters. This knowledge can be applied to develop new synthetic methods, improve existing processes, and create novel materials with specific characteristics.
Used in Material Science:
In the field of material science, γ-Carboxyglutamic Acid γ,γ-Di-t-butyl Ester can be used to develop new polymers and materials with tailored properties. Its ability to form stable esters and its compatibility with various monomers make it a valuable component in the design and synthesis of advanced materials for various applications, such as coatings, adhesives, and composites.
Check Digit Verification of cas no
The CAS Registry Mumber 56877-44-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,8,7 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 56877-44:
(7*5)+(6*6)+(5*8)+(4*7)+(3*7)+(2*4)+(1*4)=172
172 % 10 = 2
So 56877-44-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H25NO6/c1-13(2,3)20-11(18)8(7-9(15)10(16)17)12(19)21-14(4,5)6/h8-9H,7,15H2,1-6H3,(H,16,17)
56877-44-2Relevant academic research and scientific papers
The synthesis and properties of Gla- and Phe-containing analogues of cyclic RGD pentapeptides
Davies, John S.,Enjalbal, Christine,Nguyen, Corrine,Al-Jamri, Loai,Naumer, Christian
, p. 2907 - 2915 (2007/10/03)
Cyclopentapeptides containing the Arg-Gly-Asp motif have been synthesised using solid-phase assembly of side-chain-protected linear precursors, followed by solution-phase cyclisation. The replacement of the Asp residue by γ-carboxyglutamic acid (Gla) is a novel feature which gives rise to an analogue which inhibits cell adhesion, yet its congeners do not show activity in binding assays with recombinant integrin receptors. NMR techniques support a β/γ-turn conformation in most of the analogues. The Royal Society of Chemistry 2000.
