186203-81-6 Usage
Uses
Used in Pharmaceutical Industry:
6H-Pyrrolo[3,4-b]pyridine-6-carboxylic acid, octahydro-, 1,1-diMethylethyl ester is used as a key intermediate in the synthesis of various pharmaceutical compounds for its potential biological activity and pharmacological properties. Its unique structure allows it to be a promising candidate for the development of new drugs with novel mechanisms of action.
Used in Medicinal Research:
In the field of medicinal research, 6H-Pyrrolo[3,4-b]pyridine-6-carboxylic acid, octahydro-, 1,1-diMethylethyl ester serves as a valuable tool for studying the structure-activity relationships of various drug candidates. Its unique chemical properties enable researchers to explore its potential interactions with biological targets, contributing to the advancement of drug discovery and development.
Used in Drug Design and Optimization:
6H-Pyrrolo[3,4-b]pyridine-6-carboxylic acid, octahydro-, 1,1-diMethylethyl ester is utilized in drug design and optimization processes to improve the pharmacokinetic and pharmacodynamic profiles of drug candidates. Its unique structural features can be exploited to enhance the potency, selectivity, and safety of new therapeutic agents.
Used in Chemical Synthesis:
In the realm of chemical synthesis, 6H-Pyrrolo[3,4-b]pyridine-6-carboxylic acid, octahydro-, 1,1-diMethylethyl ester is employed as a versatile building block for the creation of diverse chemical libraries. Its reactivity and functional groups make it suitable for various synthetic transformations, facilitating the exploration of novel chemical space for potential drug leads.
Used in Biochemical Assays and Screening:
6H-Pyrrolo[3,4-b]pyridine-6-carboxylic acid, octahydro-, 1,1-diMethylethyl ester is utilized in biochemical assays and high-throughput screening campaigns to identify and evaluate its potential as a modulator of specific biological targets. Its unique chemical properties allow it to be a valuable probe for understanding the mechanisms of action and potential therapeutic applications in various disease states.
Overall, 6H-Pyrrolo[3,4-b]pyridine-6-carboxylic acid, octahydro-, 1,1-diMethylethyl ester is a versatile and promising compound with a wide range of applications in the pharmaceutical and research industries, driven by its unique structure, potential biological activity, and diverse uses in drug development and chemical synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 186203-81-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,6,2,0 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 186203-81:
(8*1)+(7*8)+(6*6)+(5*2)+(4*0)+(3*3)+(2*8)+(1*1)=136
136 % 10 = 6
So 186203-81-6 is a valid CAS Registry Number.
186203-81-6Relevant articles and documents
AMINOQUINAZOLINE DERIVATIVES AND THEIR SALTS AND METHODS OF USE
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, (2014/08/19)
The present invention relates to the field of medicine. Provided herein are aminoquinazoline derivatives, their salts and pharmaceutical formulations useful in modulating the protein tyrosine kinase activity, and in modulating inter- and/or intra-cellular signaling. Also provided herein are pharmaceutically acceptable compositions comprising the aminoquinazoline compounds and methods of using the compositions in the treatment of hyperproliferative disorders in mammals, especially humans.
AMINOQUINAZOLINE DERIVATIVES AND THEIR SALTS AND METHODS OF USE
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, (2013/06/05)
The present invention relates to the field of medicine. Provided herein are aminoquinazoline derivatives, their salts and pharmaceutical formulations useful in modulating the protein tyrosine kinase activity, and in modulating inter-and/or intra-cellular signaling. Also provided herein are pharmaceutically acceptable compositions comprising the aminoquinazoline compounds and methods of using the compositions in the treatment of hyperproliferative disorders in mammals, especially humans.
Process for preparation of chiral 3-amino-pyrrolidine and analogous bicyclic compounds
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, (2008/06/13)
A process for the preparation of chiral 3-aminopyrrolidine and analogous bicyclic derivatives from dihydroxy olefins by treatment with titanium isopropoxide, an optically active tartrate ester and tert-butyl hydroperoxide, followed by subsequent alkylatio