82730-04-9 Usage
Uses
Used in Pharmaceutical Industry:
(2R,3R)-2-[(3S,4R)-3-Azido-2-oxo-4-((E)-styryl)-azetidin-1-yl]-3-hydroxy-butyric acid 4-nitro-benzyl ester is used as a pharmaceutical intermediate for the synthesis of complex drug molecules. Its unique structural features, including the azido and hydroxyl groups, allow for the development of novel therapeutic agents with specific biological activities.
Used in Chemical Research:
In the field of chemical research, (2R,3R)-2-[(3S,4R)-3-Azido-2-oxo-4-((E)-styryl)-azetidin-1-yl]-3-hydroxy-butyric acid 4-nitro-benzyl ester serves as a valuable compound for studying the reactivity and properties of azido and hydroxyl functional groups. Its complex structure provides a platform for exploring new reaction pathways and mechanisms, contributing to the advancement of organic chemistry.
Used in Material Science:
(2R,3R)-2-[(3S,4R)-3-Azido-2-oxo-4-((E)-styryl)-azetidin-1-yl]-3-hydroxy-butyric acid 4-nitro-benzyl ester is utilized in material science for the development of new materials with specific properties. (2R,3R)-2-[(3S,4R)-3-Azido-2-oxo-4-((E)-styryl)-azetidin-1-yl]-3-hydroxy-butyric acid 4-nitro-benzyl ester's azido and hydroxyl groups can be exploited to create materials with tailored characteristics, such as improved stability, reactivity, or selectivity, for use in various applications.
Used in Biochemistry:
In biochemistry, (2R,3R)-2-[(3S,4R)-3-Azido-2-oxo-4-((E)-styryl)-azetidin-1-yl]-3-hydroxy-butyric acid 4-nitro-benzyl ester is employed as a tool for studying enzyme mechanisms and interactions. (2R,3R)-2-[(3S,4R)-3-Azido-2-oxo-4-((E)-styryl)-azetidin-1-yl]-3-hydroxy-butyric acid 4-nitro-benzyl ester's unique structure allows researchers to probe the active sites of enzymes and understand the molecular basis of their catalytic activities.
Overall, (2R,3R)-2-[(3S,4R)-3-Azido-2-oxo-4-((E)-styryl)-azetidin-1-yl]-3-hydroxy-butyric acid 4-nitro-benzyl ester is a multifaceted compound with potential applications across various industries, including pharmaceuticals, chemical research, material science, and biochemistry. Its unique structural features and functional groups make it a promising candidate for the development of innovative products and technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 82730-04-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,7,3 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 82730-04:
(7*8)+(6*2)+(5*7)+(4*3)+(3*0)+(2*0)+(1*4)=119
119 % 10 = 9
So 82730-04-9 is a valid CAS Registry Number.
82730-04-9Relevant academic research and scientific papers
N-Unsubstituted β-Lactams from β-Hydroxy-α-amino Acids. Facile Preparation of Intermediates for Isocephalosporins
Bose, Ajay K.,Manhas, M. S.,Vincent, J. E.,Gala, K.,Fernandez, I. F.
, p. 4075 - 4081 (2007/10/02)
A facile method has been devised for the synthesis of N-unsubstituted β-lactams.The cis-azido β-lactam (13) obtained by the reaction of azidoacetyl chloride and the Schiff base (10), derived from cinnamaldehyde and a threonine ester, is subjected to contr
