85-53-0 Usage
Description
(2R,3E,5R)-3-(2-hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo[3.2.0]heptane-2-carboxylic acid is a complex organic molecule characterized by a unique bicyclic ring system with a carboxylic acid functional group and a hydroxyethylidene side chain. The presence of oxoand oxamoieties in the ring structure suggests a propensity for reactive chemistry, while its azabicyclo[3.2.0]heptane derivative nature indicates a common structural motif in biologically active compounds. The specific stereochemistry (2R, 3E, 5R) contributes to its potential for diverse biochemical interactions due to its distinct 3-dimensional shape, making it a promising candidate for further investigation into its pharmacological and medicinal properties.
Uses
Used in Pharmaceutical Industry:
(2R,3E,5R)-3-(2-hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo[3.2.0]heptane-2-carboxylic acid is used as a potential pharmaceutical agent for its unique structure and biochemical interactions. (2R,3E,5R)-3-(2-hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo[3.2.0]heptane-2-carboxylic acid's oxoand oxamoieties, along with its azabicyclo[3.2.0]heptane derivative nature, suggest that it may have applications in the development of new drugs targeting specific biological pathways or receptors.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (2R,3E,5R)-3-(2-hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo[3.2.0]heptane-2-carboxylic acid serves as a valuable compound for studying its potential interactions with biological systems. Its specific stereochemistry and complex structure make it an interesting subject for exploring novel mechanisms of action and therapeutic effects.
Used in Chemical Synthesis:
(2R,3E,5R)-3-(2-hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo[3.2.0]heptane-2-carboxylic acid is utilized as a key intermediate in the synthesis of other complex organic molecules. Its reactive functional groups and unique structural features make it a versatile building block for creating new compounds with potential applications in various industries, including pharmaceuticals, materials science, and agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 85-53-0 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 85-53:
(4*8)+(3*5)+(2*5)+(1*3)=60
60 % 10 = 0
So 85-53-0 is a valid CAS Registry Number.
85-53-0Relevant articles and documents
BROMINATION OF 2-BENZOYLBENZOIC ACIDS
Popov, S.I.,Kopylova, T.M.,Andrievskii, A.M.,Medvedev, S.V.,Yatsenko, A.V.
, p. 279 - 285 (2007/10/02)
A new method was developed for the synthesis of bromine-substituted 9,10-anthraquinones by bromination of 2-benzoylbenzoic acid derivatives in the presence of sulfuric and nitric acids followed by cyclization.
