150722-68-2 Usage
Description
(S)-2-<(tert-butoxycarbonyl)amino>-6-phenylhexanoic acid is a chiral compound characterized by a molecular formula of C19H29NO4. It features a tert-butoxycarbonyl (Boc) protecting group on the amino group and a phenyl group attached to the carbon chain. (S)-2-<(tert-butoxycarbonyl)amino>-6-phenylhexanoic acid is widely recognized for its utility as a building block in organic synthesis and is frequently utilized in the pharmaceutical industry as an intermediate for the production of various drugs. Its chiral nature renders it particularly valuable in the synthesis of enantiomerically pure compounds, and the structural versatility allows for the creation of diverse chemical compounds with a range of properties and functions. Consequently, (S)-2-<(tert-butoxycarbonyl)amino>-6-phenylhexanoic acid holds a broad spectrum of applications across the fields of chemistry and pharmaceuticals.
Uses
Used in Pharmaceutical Industry:
(S)-2-<(tert-butoxycarbonyl)amino>-6-phenylhexanoic acid is used as a key intermediate for the synthesis of various drugs, leveraging its chiral properties to produce enantiomerically pure compounds. This is crucial in the development of more effective and safer medications, as the different enantiomers of a drug can have significantly different effects on the body.
Used in Organic Synthesis:
In the realm of organic synthesis, (S)-2-<(tert-butoxycarbonyl)amino>-6-phenylhexanoic acid serves as a versatile building block. Its structure, which includes a Boc-protected amino group and a phenyl group, allows for the creation of a wide array of chemical compounds with diverse properties and potential applications.
Used in Research and Development:
(S)-2-<(tert-butoxycarbonyl)amino>-6-phenylhexanoic acid is also employed in research and development settings, where its unique structural features and reactivity can be explored to understand new chemical reactions and develop innovative synthetic pathways.
Used in Chemical Industry:
Within the chemical industry, (S)-2-<(tert-butoxycarbonyl)amino>-6-phenylhexanoic acid can be utilized to produce specialty chemicals, materials, or other compounds that may have specific applications in various sectors, such as agriculture, materials science, or environmental technology.
Check Digit Verification of cas no
The CAS Registry Mumber 150722-68-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,7,2 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 150722-68:
(8*1)+(7*5)+(6*0)+(5*7)+(4*2)+(3*2)+(2*6)+(1*8)=112
112 % 10 = 2
So 150722-68-2 is a valid CAS Registry Number.
150722-68-2Relevant articles and documents
PROCESS FOR PRODUCTION OF NONNATURAL AMINO ACIDS AND INTERMEDIATES THEREFOR
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Page/Page column 12, (2010/11/25)
A process for the preparation of a nonnatural amino acid represented by the following formula (C): which is characterized by reacting a compound represented by the following formula (A1), a compound represented by the following formula (A2) and a compoun
