552335-71-4 Usage
Uses
Used in Pharmaceutical Synthesis:
(S)-N-Boc-2-(5'-hexyl)glycine is used as a building block for the synthesis of pharmaceuticals due to its unique structural features and properties. Its versatility allows for the creation of novel drug molecules that can potentially address various medical conditions.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (S)-N-Boc-2-(5'-hexyl)glycine is used as a key component in the development of new therapies. Its properties make it an ideal candidate for the design and synthesis of innovative drug molecules that can target specific medical conditions more effectively.
Used in Drug Discovery:
(S)-N-Boc-2-(5'-hexyl)glycine is employed as a crucial element in drug discovery processes. Its unique characteristics enable researchers to explore new avenues in the development of therapeutic agents that can potentially revolutionize the treatment of various diseases.
Used in the Chemical Industry:
(S)-N-Boc-2-(5'-hexyl)glycine is used as an intermediate in the chemical industry for the production of various compounds and materials. Its unique properties make it a valuable asset in the synthesis of a wide range of products, from pharmaceuticals to specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 552335-71-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,2,3,3 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 552335-71:
(8*5)+(7*5)+(6*2)+(5*3)+(4*3)+(3*5)+(2*7)+(1*1)=144
144 % 10 = 4
So 552335-71-4 is a valid CAS Registry Number.
552335-71-4Relevant academic research and scientific papers
Asymmetric Synthesis of Protected Unnatural α-Amino Acids via Enantioconvergent Nickel-Catalyzed Cross-Coupling
Freas, Dylan J.,Fu, Gregory C.,Yang, Ze-Peng
, p. 8614 - 8618 (2021/06/28)
Interest in unnatural α-Amino acids has increased rapidly in recent years in areas ranging from protein design to medicinal chemistry to materials science. Consequently, the development of efficient, versatile, and straightforward methods for their enanti
CALPAIN MODULATORS AND METHODS OF PRODUCTION AND USE THEREOF
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, (2017/09/27)
The present technology relates to compounds, kits, compositions, and methods useful for the treatment of fibrotic disease. In some aspects, the present technology provides for treatment of various diseases or disorders associated or mediated, at least in part, by calpains, such as CAPN1, CAPN2, and/or CAPN9. The present technology is generally applicable to compounds which inhibit myofibroblast differentiation.
Bicyclic tetrapeptides as potent HDAC inhibitors: Effect of aliphatic loop position and hydrophobicity on inhibitory activity
Islam, Md. Nurul,Islam, Md. Shahidul,Hoque, Md. Ashraful,Kato, Tamaki,Nishino, Norikazu,Ito, Akihiro,Yoshida, Minoru
, p. 3862 - 3870 (2014/08/18)
Several histone deacetylase (HDAC) inhibiting bicyclic tetrapeptides have been designed and synthesized through intramolecular ring-closing metathesis (RCM) reaction and peptide cyclization. We designed bicyclic tetrapeptides based on CHAP31, trapoxin B a
