94835-25-3 Usage
Uses
Used in Chemical Synthesis:
L-Leucine, N-[N-[(1,1-dimethylethoxy)carbonyl]-L-alanyl]-, 2-(diphenylphosphino)ethyl ester is used as a reagent in chemical synthesis for its ability to facilitate the formation of specific chemical bonds and reactions. Its unique structure allows for the creation of novel compounds with potential applications in various fields.
Used in Peptide Chemistry:
In peptide chemistry, L-Leucine, N-[N-[(1,1-dimethylethoxy)carbonyl]-L-alanyl]-, 2-(diphenylphosphino)ethyl ester is used as a building block for the synthesis of peptides and proteins. Its ester functionality enables the formation of peptide bonds, which are essential for the construction of larger peptide chains.
Used in Protein Modification:
L-Leucine, N-[N-[(1,1-dimethylethoxy)carbonyl]-L-alanyl]-, 2-(diphenylphosphino)ethyl ester is used as a protein-modifying agent to study the structure and function of proteins. By attaching L-Leucine, N-[N-[(1,1-dimethylethoxy)carbonyl]-L-alanyl]-,
2-(diphenylphosphino)ethyl ester to specific amino acid residues, researchers can investigate the effects of structural modifications on protein stability, folding, and function.
Used in Drug Development:
In the field of drug development, L-Leucine, N-[N-[(1,1-dimethylethoxy)carbonyl]-L-alanyl]-, 2-(diphenylphosphino)ethyl ester is used as a potential lead compound for the development of new drugs and therapies. Its unique structure and functional groups may provide novel mechanisms of action or improve the pharmacokinetic properties of existing drugs.
Used in Pharmacological Research:
L-Leucine, N-[N-[(1,1-dimethylethoxy)carbonyl]-L-alanyl]-, 2-(diphenylphosphino)ethyl ester is used in pharmacological research to study the interactions between drugs and biological targets. Its ability to modify proteins and peptides allows researchers to investigate the binding affinity, selectivity, and mechanism of action of potential drug candidates.
Used in Biotechnology:
In biotechnology, L-Leucine, N-[N-[(1,1-dimethylethoxy)carbonyl]-L-alanyl]-, 2-(diphenylphosphino)ethyl ester is used for the development of new biotechnological applications, such as the creation of biosensors, enzyme inhibitors, or other bioactive molecules. Its unique structure and functional groups may provide novel properties and applications in this field.
Used in Pharmaceutical Industry:
L-Leucine, N-[N-[(1,1-dimethylethoxy)carbonyl]-L-alanyl]-, 2-(diphenylphosphino)ethyl ester is used in the pharmaceutical industry as a key intermediate in the synthesis of various drug candidates. Its unique structure and reactivity make it a valuable component in the development of new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 94835-25-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,8,3 and 5 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 94835-25:
(7*9)+(6*4)+(5*8)+(4*3)+(3*5)+(2*2)+(1*5)=163
163 % 10 = 3
So 94835-25-3 is a valid CAS Registry Number.
94835-25-3Relevant academic research and scientific papers
THE 2-(DIPHENYLPHOSPHINO)ETHYL GROUP (DPPE) AS A NEW CARBOXYL-PROTECTING GROUP IN PEPTIDE CHEMISTRY
Chantreux, Dominique,Gamet, Jean-Paul,Jacquier, Robert,Verducci, Jean
, p. 3087 - 3094 (2007/10/02)
The use of 2-(diphenylphosphino)ethyl group for carboxyl-protection of amino acids or peptides is described.This group is easily introduced by esterification using 2-(diphenylphosphino)ethanol in the presence of dicyclohexylcarbodiimide and 4-(dimethylamino)pyridine.These Dppe esters are stable under the standard conditions for peptide synthesis.Deprotection is carried out under mild conditions by quaternisation using methyl iodide followed by a β-elimination induced by fluoride ion or potassium carbonate.
