93779-30-7 Usage
Description
(+/-)-Octahydrocyclopenta[b]pyrrole-2-carboxylic acid hydrochloride is an organic compound with a unique cyclic structure, featuring a hydrochloride salt form. It is characterized by its octahydrocyclopenta[b]pyrrole core, which is a fused ring system composed of five carbon atoms and one nitrogen atom. The carboxylic acid group at the 2-position provides it with acidic properties, making it a versatile molecule for various applications in the pharmaceutical and chemical industries.
Uses
Used in Pharmaceutical Research:
(+/-)-Octahydrocyclopenta[b]pyrrole-2-carboxylic acid hydrochloride is used as a research compound for the study of angiotensin-converting enzyme (ACE) inhibitors. ACE inhibitors are a class of drugs that are used to treat hypertension and heart failure by blocking the conversion of angiotensin I to angiotensin II, a potent vasoconstrictor. The unique structure of this compound allows researchers to investigate its potential as a lead molecule in the development of new ACE inhibitors.
Used in Chemical Synthesis:
In the chemical industry, (+/-)-Octahydrocyclopenta[b]pyrrole-2-carboxylic acid hydrochloride can be used as a building block or intermediate in the synthesis of more complex organic molecules. Its carboxylic acid functionality can be used to form esters, amides, or other derivatives, making it a valuable component in the creation of pharmaceuticals, agrochemicals, or other specialty chemicals.
Used in Drug Design:
The octahydrocyclopenta[b]pyrrole core of (+/-)-Octahydrocyclopenta[b]pyrrole-2-carboxylic acid hydrochloride can serve as a structural motif in drug design. Its unique fused ring system and carboxylic acid group can be exploited to design new drugs with improved pharmacokinetic and pharmacodynamic properties. Researchers can modify the molecule by adding various functional groups or substituents to optimize its binding affinity, selectivity, and efficacy for specific biological targets.
Check Digit Verification of cas no
The CAS Registry Mumber 93779-30-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,7,7 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 93779-30:
(7*9)+(6*3)+(5*7)+(4*7)+(3*9)+(2*3)+(1*0)=177
177 % 10 = 7
So 93779-30-7 is a valid CAS Registry Number.
93779-30-7Relevant articles and documents
A PROCESS FOR PREPARATION OF RAMIPRIL
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Page/Page column 11, (2009/10/30)
Disclosed herein is a process for preparation of Ramipril; which comprises; reacting salts of (S,S,S)-azabicyclo[3.3.0]-octane-3-carboxylate with N-[l-(S)-ethoxy carbonyl)-3- phenyl propyl] -L-alanine in presence of dicyclohexylcarbodimide (DCC) and 1- hydroxybenzotriazole (HOBT) in a suitable solvent medium.
SYNTHESIS OF UNNATURAL AMINO ACIDS: (S,S,S)-2-AZABICYCLOOCTANE-3-CARBOXYLIC ACID
Teetz, V.,Geiger, R.,Gaul, H.
, p. 4479 - 4482 (2007/10/02)
(S,S,S)-2-Azabicyclooctane-3-carboxylic acid 1, a structural element of the very potent ACE inhibitor HOE 498, is readily available via a diastereo selective synthesis starting from serine or cystine.
