90580-95-3 Usage
Bicyclic structure
The compound has a bicyclic structure, which means it consists of two rings of atoms connected to each other.
Carboxylic acid
The compound contains a carboxylic acid functional group, which is characterized by the presence of a carbonyl group (C=O) and a hydroxyl group (-OH) attached to the same carbon atom.
Nitrophenyl methyl ester group
The compound has a nitrophenyl methyl ester group, which is an ester derived from a nitrophenol and a methyl alcohol.
Acetylaminoethylthio functional group
The compound contains an acetylaminoethylthio functional group, which is characterized by the presence of an acetylamino group (-NHCOCH3) and an ethylthio group (-SCH2CH3).
Hydroxyisopropyl functional group
The compound also has a hydroxyisopropyl functional group, which is an isopropyl group (-CH(CH3)2) with a hydroxyl group (-OH) attached to it.
Cis configuration
The compound is in a cis configuration, which means that the functional groups are on the same side of the molecule.
Unique structure
The compound has a unique structure due to the presence of various functional groups and its bicyclic nature.
Potential applications
The compound has various potential applications due to its unique structure and functional groups, which can be exploited in different fields such as pharmaceuticals, materials science, and chemical research.
Check Digit Verification of cas no
The CAS Registry Mumber 90580-95-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,5,8 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 90580-95:
(7*9)+(6*0)+(5*5)+(4*8)+(3*0)+(2*9)+(1*5)=143
143 % 10 = 3
So 90580-95-3 is a valid CAS Registry Number.
90580-95-3Relevant academic research and scientific papers
Synthesis of 5,6-cis-Carbapenems Related to C-19393 H2
Natsugari, Hideaki,Matsushita, Yoshihiro,Tamura, Norikazu,Yoshioka, Kouichi,Ochiai, Michihiko
, p. 403 - 412 (2007/10/02)
The synthesis of 6,7-cis-7-(1-hydroxy-1-methylethyl)-3-oxa-1-azabicyclooctan-8-ones (3a, b), key intermediates for the preparation of the 5,6-cis-carbapenem antibiotic C-19393 H2
