176237-45-9 Usage
Uses
Used in Pharmaceutical Applications:
L-Norvaline, 5-[(methylsulfonyl)oxy]-N-[(phenylmethoxy)carbonyl]-, 1-methylethyl ester is used as a therapeutic agent for its anti-inflammatory and antioxidant properties. It may contribute to the treatment of various conditions by reducing inflammation and oxidative stress, which are common factors in many diseases.
Used in Organic Synthesis:
In the field of organic synthesis, L-Norvaline, 5-[(methylsulfonyl)oxy]-N-[(phenylmethoxy)carbonyl]-, 1-methylethyl ester is used as a building block or intermediate for the synthesis of more complex organic compounds. Its unique structure allows for the development of novel chemical entities with potential applications in various industries.
Used in Drug Discovery:
L-Norvaline, 5-[(methylsulfonyl)oxy]-N-[(phenylmethoxy)carbonyl]-, 1-methylethyl ester is used as a lead compound in drug discovery. Its unique chemical structure and potential biological activities make it a promising candidate for further research and development into new pharmaceuticals.
Used in Chemical Research:
In the field of chemical research, L-Norvaline, 5-[(methylsulfonyl)oxy]-N-[(phenylmethoxy)carbonyl]-, 1-methylethyl ester is used as a subject of study to explore its properties, reactivity, and potential applications. This research can lead to a better understanding of its behavior and the development of new methods for its synthesis and use.
Check Digit Verification of cas no
The CAS Registry Mumber 176237-45-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,2,3 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 176237-45:
(8*1)+(7*7)+(6*6)+(5*2)+(4*3)+(3*7)+(2*4)+(1*5)=149
149 % 10 = 9
So 176237-45-9 is a valid CAS Registry Number.
InChI:InChI=1/C17H25NO7S/c1-13(2)25-16(19)15(10-7-11-24-26(3,21)22)18-17(20)23-12-14-8-5-4-6-9-14/h4-6,8-9,13,15H,7,10-12H2,1-3H3,(H,18,20)/t15-/m0/s1
176237-45-9Relevant academic research and scientific papers
Enantioselective syntheses of (R)- and (S)-hexahydropyridazine-3-carboxylic acid derivatives
Schmidt, Ulrich,Braun, Christine,Sutoris, Heinz
, p. 223 - 229 (2007/10/03)
Appropriately protected optically active tetrahydropyridazine-3-carboxylic acid and hexahydropyridazine-3-carboxylic acid were prepared via ring closure of α-hydrazino- and δ-hydrazinopentanoates. Either optically active glutamic acid or an enantioselective catalytic hydrogenation was used to generate the chiral center. The numerous optically active intermediates are valuable starting materials for the synthesis of other unusual amino acids.
