47312-26-5 Usage
Uses
Used in Pharmaceutical Industry:
(S)-2-Benzyloxycarbonylamino-heptanedioic acid 7-methyl ester is used as a building block for the synthesis of complex organic molecules, particularly in the development of new pharmaceutical drugs. Its benzyloxycarbonylamino group provides versatility in peptide chemistry, allowing for the creation of diverse molecular structures with potential therapeutic applications.
Used in Biochemical Research:
In the field of biochemistry, (S)-2-Benzyloxycarbonylamino-heptanedioic acid 7-methyl ester serves as a valuable tool for researchers. Its unique structure allows for exploration into various biochemical interactions and mechanisms, potentially leading to advancements in understanding biological processes and the development of novel bioactive compounds.
Further research and testing are necessary to fully comprehend the potential applications and to thoroughly investigate the properties and effects of (S)-2-Benzyloxycarbonylamino-heptanedioic acid 7-methyl ester. As our understanding of (S)-2-Benzyloxycarbonylamino-heptanedioic acid 7-methyl ester grows, so too may its utility in various industries, particularly in the development of innovative pharmaceuticals and biochemistry applications.
Check Digit Verification of cas no
The CAS Registry Mumber 47312-26-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,7,3,1 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 47312-26:
(7*4)+(6*7)+(5*3)+(4*1)+(3*2)+(2*2)+(1*6)=105
105 % 10 = 5
So 47312-26-5 is a valid CAS Registry Number.
47312-26-5Relevant academic research and scientific papers
Inhibitors selective for HDAC6 in enzymes and cells
Gupta, Praveer K.,Reid, Robert C.,Liu, Ligong,Lucke, Andrew J.,Broomfield, Steve A.,Andrews, Melanie R.,Sweet, Matthew J.,Fairlie, David P.
supporting information; experimental part, p. 7067 - 7070 (2011/01/03)
Histone deacetylase inhibitors with anticancer or anti-inflammatory activity bind to Class I or Class I and II HDAC enzymes. Here we compare selectivity of inhibitors of a Class II HDAC enzyme (HDAC6) and find one that retains high selectivity in macrophages.
Practical and efficient enantioselective synthesis of α-amino acids in aqueous media
Suarez, Rosa M.,Sestelo, Jose Perez,Sarandeses, Luis A.
, p. 3584 - 3587 (2007/10/03)
Enantiomerically pure natural and unnatural α-amino acids have been synthesized from a chiral melhyleneoxazolidinone by means of a highly diastereoselective 1,4-conjugate addition of alkyl iodides in aqueous media. The zinc-copper conjugate addition reaction exhibits high chemoselectivity, with the possibility of using functionalized iodides, to afford a single diastereomer in short reaction times and with good yields.
