394653-46-4Relevant academic research and scientific papers
HETEROARYL BTK INHIBITORS
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Page/Page column 121, (2011/04/14)
The present invention provides compounds useful as inhibitors of Btk, compositions thereof, and methods of using the same.
(S)-2-amino-2-(oxetan-3-yl)acetic acid, also known as S-3-oxetanylalanine, is a unique amino acid derivative characterized by its molecular formula C6H9NO3. (S)-2-amino-2-(oxetan-3-yl)acetic acid features an unusual oxetanyl group, which is a three-membered cyclic ether, making it a subject of interest in the fields of organic and medicinal chemistry. Its distinctive structure and potential biological activity have garnered attention for its use in various applications.
394653-46-4
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Basic information
- Product Name: (S)-2-amino-2-(oxetan-3-yl)acetic acid
- Synonyms: (S)-2-amino-2-(oxetan-3-yl)acetic acid
- CAS NO:394653-46-4
- Molecular Formula: C5H9NO3
- Molecular Weight: 131.12986
- EINECS: N/A
- Product Categories: N/A
- Mol File: 394653-46-4.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: /
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: (S)-2-amino-2-(oxetan-3-yl)acetic acid(CAS DataBase Reference)
- NIST Chemistry Reference: (S)-2-amino-2-(oxetan-3-yl)acetic acid(394653-46-4)
- EPA Substance Registry System: (S)-2-amino-2-(oxetan-3-yl)acetic acid(394653-46-4)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 394653-46-4(Hazardous Substances Data)
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394653-46-4 Usage
Uses
Used in Pharmaceutical Synthesis:(S)-2-amino-2-(oxetan-3-yl)acetic acid is used as a building block for the synthesis of novel pharmaceuticals, leveraging its unique structure to create innovative and potentially effective medications.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (S)-2-amino-2-(oxetan-3-yl)acetic acid serves as a valuable tool for studying the structure-activity relationships of biological molecules, contributing to the understanding of how these molecules interact with their targets and potentially leading to the development of new therapeutic agents.
Used in Material Science:
(S)-2-amino-2-(oxetan-3-yl)acetic acid has potential applications in material science, where its unique properties may be harnessed to create new materials with specific characteristics or functions.
Used as a Chiral Ligand in Asymmetric Synthesis:
In the realm of asymmetric synthesis, (S)-2-amino-2-(oxetan-3-yl)acetic acid is utilized as a chiral ligand, playing a crucial role in the selective synthesis of enantiomerically pure compounds, which are essential in the production of many pharmaceuticals and agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 394653-46-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,4,6,5 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.Calculate Digit Verification of CAS Registry Number 394653-46:
(8*3)+(7*9)+(6*4)+(5*6)+(4*5)+(3*3)+(2*4)+(1*6)=184
184 % 10 = 4
So 394653-46-4 is a valid CAS Registry Number.
394653-46-4Upstream product
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(S)-2-amino-2-(oxetan-3-yl)acetic acid
