6238-34-2 Usage
Description
Quinuclidine-3-carboxylic acid hydrochloride is a chemical compound that serves as a salt form of quinuclidine-3-carboxylic acid, a heterocyclic amine derivative. It is recognized for its potential pharmaceutical applications and is utilized as a building block in the synthesis of various pharmaceutical compounds.
Uses
Used in Pharmaceutical Industry:
Quinuclidine-3-carboxylic acid hydrochloride is used as a precursor in the preparation of medicinally important molecules, contributing to the development of drugs for the treatment of various medical conditions.
Used as a Chiral Auxiliary in Chemical Synthesis:
Quinuclidine-3-carboxylic acid hydrochloride is employed as a chiral auxiliary, which is instrumental in chemical synthesis to control the stereochemistry of reactions, leading to the production of enantiomerically pure compounds.
Used in Organic Chemistry:
Quinuclidine-3-carboxylic acid hydrochloride is an important reagent in organic chemistry, facilitating a range of chemical reactions and processes, thereby enhancing the synthesis of complex organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 6238-34-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,3 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6238-34:
(6*6)+(5*2)+(4*3)+(3*8)+(2*3)+(1*4)=92
92 % 10 = 2
So 6238-34-2 is a valid CAS Registry Number.
6238-34-2Relevant articles and documents
SYNTHESIS OF 1,3-DIMETHYL-8-(QUINUCLID-3-YL)XANTHINE AND ITS INVESTIGATION
Zhichareva, G. P.,Yakhontov, L. N.,Marshalkin, M. F.,Turchin, K. F.,Kuleshova, E. F.,Sheinker, Yu. N.
, p. 22 - 26 (1991)
-
Synthesis and Muscarinic Activities of Quinuclidin-3-yltriazole and -tetrazole Derivatives
Wadsworth, Harry J.,Jenkins, Sarah M.,Orlek, Barry S.,Cassidy, Frederick,Clark, Michael S. G.,et al.
, p. 1280 - 1290 (2007/10/02)
The synthesis of 15 methyl or unsubstituted 1,2,3-triazoles, 1,2,4-triazoles, and tetrazoles additionally substituted with a 1-azabicyclooctan-3-yl group is described.The potency and efficacy of these compounds as muscarinic ligands were determined in radioligand binding assays using oxotremorine and quinuclidinyl benzilate.Potency and efficacy were found in compounds in which the azole moiety was attached to the azabicyclic ring either through a carbon atom or a nitrogen atom.Electrostatic potential maps of both the C-linked and the novel N-linked series of compounds were calculated.A relationship between position and depth of the electrostatic minima relative to the azabicyclic ring and the potency and efficacy of the compounds was determined.