56972-71-5 Usage
Uses
Used in Pharmaceutical Industry:
2-(benzyloxy)-3-methylbutanoic acid is used as a precursor in the synthesis of various drugs and pharmaceutical products. Its unique structure allows for the development of new compounds with potential therapeutic effects.
Used in Research and Development:
In the field of research and development, 2-(benzyloxy)-3-methylbutanoic acid serves as a building block for the creation of new chemical compounds. Its versatile structure enables scientists to explore its potential in forming novel molecules with specific properties and applications.
Used in Organic Synthesis:
2-(benzyloxy)-3-methylbutanoic acid is utilized in organic synthesis for the preparation of a wide range of organic compounds. Its functional groups and structural features make it a valuable intermediate in the synthesis of various organic molecules.
Used in Chemical Engineering:
In the field of chemical engineering, 2-(benzyloxy)-3-methylbutanoic acid may have potential applications in the development of new materials, catalysts, or processes. Its unique structure and reactivity can contribute to advancements in chemical engineering technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 56972-71-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,9,7 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 56972-71:
(7*5)+(6*6)+(5*9)+(4*7)+(3*2)+(2*7)+(1*1)=165
165 % 10 = 5
So 56972-71-5 is a valid CAS Registry Number.
56972-71-5Relevant academic research and scientific papers
Asymmetric synthesis of β-hydroxy acid via stereoselective dirhodium(II)-catalyzed C-H insertion of α-alkoxydiazoketone
Yakura, Takayuki,Tanaka, Takeshi,Ikeda, Masazumi,Uenishi, Jun'ichi
, p. 471 - 473 (2007/10/03)
A new methodology for the asymmetric synthesis of β-hydroxy acid was developed. Dirhodium(II)-catalyzed C-H insertion of α-alkoxydiazoketone (3), which was prepared from primary alkyl halide (1) and readily available chiral α-hydroxy acid (2), gave stereo
