193267-93-5 Usage
Molecular structure
The compound consists of a pyrrolidine ring, a carboxylic acid functional group, a nitrophenyl group, and an ester linkage.
Stereochemistry
The compound has a (2S) configuration, indicating the presence of a chiral center with a specific spatial arrangement of the substituents.
Functional groups
The compound contains a carboxylic acid group (-COOH) and an ester group (-COO-).
Nitrophenyl group
A 4-nitrophenyl group is present, which is characterized by a nitro (-NO2) functional group attached to a phenyl ring.
Pyrrolidine ring
The compound features a five-membered nitrogen-containing heterocyclic ring, which is a key structural component.
Dimethylethoxycarbonyl group
A (1,1-dimethylethoxy)carbonyl group is attached to the pyrrolidine ring, which consists of a carbonyl group (C=O) flanked by two methyl groups and an ethoxy group (-OCH3).
Amino group
The compound contains an amino group (-NH2) that is connected to the pyrrolidine ring through a carbonyl group.
Synthetic compound
This compound is synthetic, meaning it is not found naturally in the environment and is typically produced through chemical synthesis.
Research and pharmaceutical applications
Due to its unique structure and properties, the compound may have potential applications in drug development and other scientific fields.
Complexity
The compound is a complex molecule with multiple functional groups and stereochemistry, which may contribute to its potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 193267-93-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,2,6 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 193267-93:
(8*1)+(7*9)+(6*3)+(5*2)+(4*6)+(3*7)+(2*9)+(1*3)=165
165 % 10 = 5
So 193267-93-5 is a valid CAS Registry Number.
193267-93-5Relevant articles and documents
Process for producing 1H-3-aminopyrrolidine and derivatives thereof
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Page 20, (2008/06/13)
A process for producing 1H-3-aminopyrrolidine and derivatives thereof is disclosed. The process is especially useful for producing optically active 1H-3-aminopyrrolidine and derivatives thereof and in this case comprises reacting an optically active amino-protected aspartic anhydride represented by the formula (1) with a primary amine represented by the formula R'NH2, subjecting the reaction product to cyclodehydration to obtain an optically active 1-aralkyl-3-(protected amino)pyrrolidine-2,5-dione compound represented by the formula (2), subsequently eliminating the protective group from the 3-position amino group of the compound represented by the formula (2) to obtain an optically active 1-aralkyl-3-aminopyrrolidine-2,5-dione compound represented by the formula (3), reducing the carbonyl groups of the compound represented by the formula (3) to obtain either an optically active 1-aralkyl-3-aminopyrrolidine compound represented by the formula (4) or a salt thereof with a protonic acid, and then subjecting the compound represented by the formula (4) or the salt thereof to hydrogenolysis to obtain an optically active 1H-3-aminopyrrolidine or a protonic acid salt thereof.
