53623-87-3 Usage
Description
(S)-3-(benzyloxycarbonyl)-5-oxo-4-oxazolidineacetic acid is a chemical compound belonging to the oxazolidine family, characterized by a five-membered heterocyclic ring containing oxygen and nitrogen atoms. This specific compound features a benzyloxycarbonyl group, an oxo group on the oxazolidine ring, and a carboxylic acid moiety, making it a versatile building block for the synthesis of complex molecules, particularly in the development of new drugs and pharmaceuticals. Its unique structure and reactivity also contribute to the exploration of novel chemical reactions and mechanisms, with potential applications in both the chemical and pharmaceutical fields.
Uses
Used in Pharmaceutical Research:
(S)-3-(benzyloxycarbonyl)-5-oxo-4-oxazolidineacetic acid is used as a building block for the synthesis of complex molecules in pharmaceutical research. Its unique structure and reactivity allow for the development of new drugs and pharmaceuticals, contributing to advancements in the field.
Used in Organic Synthesis:
In the field of organic synthesis, (S)-3-(benzyloxycarbonyl)-5-oxo-4-oxazolidineacetic acid is used as a versatile intermediate for creating more complex molecules. Its functional groups enable it to be a valuable tool in exploring novel chemical reactions and mechanisms, furthering the understanding and development of organic chemistry.
Used in Drug Development:
(S)-3-(benzyloxycarbonyl)-5-oxo-4-oxazolidineacetic acid is employed as a key component in the development of new drugs. Its presence in the synthesis process allows for the creation of molecules with potential therapeutic properties, enhancing the possibilities for treating various medical conditions.
Used in Chemical Reaction Exploration:
(S)-3-(benzyloxycarbonyl)-5-oxo-4-oxazolidineacetic acid is used as a valuable tool for exploring novel chemical reactions and mechanisms in the field of chemistry. Its unique structure and reactivity provide insights into new pathways and processes, contributing to the overall knowledge and advancements in the discipline.
Check Digit Verification of cas no
The CAS Registry Mumber 53623-87-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,2 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 53623-87:
(7*5)+(6*3)+(5*6)+(4*2)+(3*3)+(2*8)+(1*7)=123
123 % 10 = 3
So 53623-87-3 is a valid CAS Registry Number.
53623-87-3Relevant articles and documents
DNA Methyltransferase inhibitors
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Page 15-16, (2008/06/13)
A compound of the formula or a pharmaceutically acceptable salt thereof,whereinR1, R2, and R3 are the same or different and are independently hydrogen, lower alkyl, aryl or substituted aryl, lower alkoxy, lower alkoxyalkyl, or cycloalkyl or cycloalkyl alkoxy, where each cycloalkyl group has from 3-7 members, where up to two of the cycloalkyl members are optionally hetero atoms selected from oxygen and nitrogen, and where any member of the alkyl, aryl or cycloalkyl group is optionally substituted with halogen, lower alkyl or lower alkoxy, aryl or substituted aryl, andwhereR3 can be ribose, deoxyribose or phosphorylated derivatives thereof,whereinR1, R2, and R3 are not all hydrogen andwhereinwhen R3 is ribose, deoxyribose or phosphorylated derivatives thereof, one of R1 or R2 is not hydrogen.
