6341-49-7 Usage
Main Properties
1. Chemical Name: 2-amino-2-ethylheptanoic acid
2. Alternate Name: α-ethyl-2-aminocaproic acid
3. Chemical Formula: \textC8\textH17\textNO2
4. Molecular Weight: 159.23 g/mol
5. Category: Amino acid derivative
6. Structure: Derivative of lysine, with an ethyl group replacing the amino group on the second carbon atom.
Specific Content
1. Chemical Composition: Contains carbon, hydrogen, nitrogen, and oxygen atoms.
2. Applications in Pharmaceutical Industry:
Pharmaceutical Intermediate: Used in the synthesis of various pharmaceutical compounds.
Chiral Building Block: Serves as a building block for the synthesis of drugs with specific chirality.
3. Medical Research and Development:
Treatment of Diseases: Investigated for potential applications in treating cancer and cardiovascular disorders.
Drug Development: Used in research and development of new pharmaceuticals.
4. Potential Uses:
Medicinal: Potential as an active pharmaceutical ingredient (API) or intermediate in drug synthesis.
Biotechnological: Possible applications in biotechnology and drug discovery.
Chemical: Employed in chemical reactions for the production of targeted compounds.
This compound's structure and properties make it valuable in pharmaceutical synthesis and medical research, particularly due to its potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 6341-49-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,4 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6341-49:
(6*6)+(5*3)+(4*4)+(3*1)+(2*4)+(1*9)=87
87 % 10 = 7
So 6341-49-7 is a valid CAS Registry Number.
6341-49-7Relevant articles and documents
Chiral, fully extended helical peptides
Crisma, Marco,Moretto, Alessandro,Peggion, Cristina,Panella, Lavinia,Kaptein, Bernard,Broxterman, Quirinus B.,Formaggio, Fernando,Toniolo, Claudio
, p. 629 - 641 (2012/06/29)
The synthesis of the N-protected (blocked) homo-peptide esters from the chiral Cα-ethyl, Cα-n-pentylglycine was performed in solution to the hexapeptide level. The conformational propensity exhibited by these oligomers in chloroform solution and in the crystal state was assessed by use of FTIR absorption, NMR, and X-ray diffraction. The results indicated that fully extended helical structures (2.05-helices) are overwhelmingly adopted irrespective of the peptide main-chain length. This oligomeric series is of great interest as it is characterized by the longest C i α,H, C i+1 α (per residue) separation achievable in the class of chiral, rigid, helical peptide spacers based on α-amino acids.
