73821-95-1 Usage
Description
Boc-Asp(Ochx)-OH, also known as Boc-L-Asp(OcHx)-OH, is an aspartic acid derivative characterized by its white to off-white powder form. It is a significant compound in the field of chemical synthesis and peptide chemistry due to its unique properties and reactivity.
Uses
Used in Chemical Synthesis:
Boc-Asp(Ochx)-OH is used as a key intermediate in the synthesis of various complex molecules and pharmaceutical compounds. Its application in this field is attributed to its reactivity and ability to form stable bonds with other molecules, facilitating the creation of diverse chemical structures.
Used in Peptide Chemistry:
In peptide chemistry, Boc-Asp(Ochx)-OH serves as an essential building block for the construction of peptides and proteins. Its use in this industry is due to its compatibility with various peptide synthesis methods and its ability to contribute to the formation of specific peptide sequences with desired properties and functions.
Used in Pharmaceutical Industry:
Boc-Asp(Ochx)-OH is utilized as a crucial component in the development of new drugs and therapeutic agents. Its application in this industry is driven by its potential to enhance the efficacy and specificity of drug molecules, as well as its ability to improve the overall pharmacokinetic and pharmacodynamic profiles of the resulting compounds.
Used in Research and Development:
Boc-Asp(Ochx)-OH is also employed in research and development settings, where it is used to study the fundamental properties of aspartic acid derivatives and their interactions with other molecules. This application is important for advancing the understanding of peptide chemistry and its implications in various biological processes and disease mechanisms.
Check Digit Verification of cas no
The CAS Registry Mumber 73821-95-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,8,2 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 73821-95:
(7*7)+(6*3)+(5*8)+(4*2)+(3*1)+(2*9)+(1*5)=141
141 % 10 = 1
So 73821-95-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H25NO6/c1-15(2,3)22-14(20)16-11(9-12(17)18)13(19)21-10-7-5-4-6-8-10/h10-11H,4-9H2,1-3H3,(H,16,20)(H,17,18)/t11-/m0/s1
73821-95-1Relevant articles and documents
Structure-activity study of L-amino acid-based N-type calcium channel blockers
Seko, Takuya,Kato, Masashi,Kohno, Hiroshi,Ono, Shizuka,Hashimura, Kazuya,Takimizu, Hideyuki,Nakai, Katsuhiko,Maegawa, Hitoshi,Katsube, Nobuo,Toda, Masaaki
, p. 1901 - 1913 (2007/10/03)
Synthesis and structure-activity relationship (SAR) study of L-amino acid-based N-type calcium channel blockers are described. The compounds synthesized were evaluated for inhibitory activity against both N-type and L-type calcium channels focusing on sel
Stable polypeptides having c-AMP production enhancing activity and the use thereof
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, (2008/06/13)
Disclosed are (1) a polypeptide represented by formula (I), or a pharmaceutically acceptable amide, ester or salt thereof: wherein X is hydrogen atom; or a lower alkyl group which may be substituted with a member selected from the group consisting of hydroxy group, substituted or unsubstituted amino group, carboxyl group, carbamoyl group, and substituted or unsubstituted aromatic group; and Y is one of amino acids or peptides consisting of 1 to 16 amino acid residues counted from the N-terminal side of Leu-Ala-Ala-Val-Leu-Gly-Lys-Arg-Tyr-Lys-Gln-Arg-Val-Lys-Asn-Lys SEQ ID NO: 20, and (2) a pharmaceutical composition comprising a polypeptide represented by formula (I), or a pharmaceutically acceptable amide, ester or salt thereof, which has remarkable c-AMP activity and is useful as a nerve activating agent.
Use of Tetrabutylammonium Fluoride as a Facile Deprotecting Reagent for 4-Nitrobenzyl, 2,2,2-Trichloroethyl, and Phenacyl Esters of Amino Acids
Namikoshi, Michio,Kundu, Bijoy,Rinehart, Kenneth L.
, p. 5464 - 5466 (2007/10/02)
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