344436-49-3 Usage
Molecular structure
The compound consists of a pyrrolidinecarboxylic acid core with a hydroxy and hydroxymethyl group, an ethyl ester derivative, and an azo compound attached to a phenyl ring.
Functional groups
The presence of carboxyl, hydroxyl, and ester groups in the molecule contributes to its reactivity and ability to form hydrogen bonds.
Aromatic ring
The compound contains a phenyl ring, which is an essential part of the azo compound and contributes to its stability and chemical properties.
Chlorine and nitro substituents
The presence of a chlorine atom and a nitro group on the phenyl ring enhances the compound's reactivity and contributes to its unique chemical properties.
Optical isomerism
The compound is an optical isomer, which means it has a stereocenter at the 2nd and 4th positions, denoted by the (2S,4R)configuration. This results in different spatial arrangements of the molecule, which can lead to different properties and applications.
Potential applications
Due to its diverse functional groups and structural features, 1-Pyrrolidinecarboxylic acid, 4-hydroxy-2-(hydroxymethyl)-, 2-[[4-[(2-chloro-4-nitrophenyl)azo]phenyl]ethylamino]ethyl ester, (2S,4R)may have potential applications in various chemical and biological processes, such as catalysis, drug design, and materials science.
Stability
The compound's stability may be influenced by the presence of the aromatic ring, the diverse functional groups, and the optical isomerism, which can affect its reactivity and potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 344436-49-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,4,4,3 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 344436-49:
(8*3)+(7*4)+(6*4)+(5*4)+(4*3)+(3*6)+(2*4)+(1*9)=143
143 % 10 = 3
So 344436-49-3 is a valid CAS Registry Number.
344436-49-3Relevant articles and documents
Fluorescent quenching detection reagents and methods
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Page column 51-52, (2008/06/13)
Oligonucleotide-fluorophore-quencher conjugates wherein the fluorophore moiety has emission wavelengths in the range of about 300 to about 800 nm, and or where the quencher includes a substituted 4-(phenyldiazenyl)phenylamine structure provide improved si
