1095223-35-0 Usage
Molecular structure
The compound has a pyrazolo[3,4-b]pyridine core structure with a carboxylic acid group, a 1,1-dimethylethyl ester group, and a hydroxymethyl group attached to the core.
Stability
The 1,1-dimethylethyl ester group on the carboxylic acid makes the compound more stable.
Bioavailability
The 1,1-dimethylethyl ester group also increases the bioavailability of the compound, making it more attractive for drug development.
Pharmacological properties
The compound has potential pharmacological properties, particularly in the field of anticancer and antiviral drugs.
Chemical modifications
The hydroxymethyl group attached to the pyrazolo[3,4-b]pyridine core provides potential sites for chemical modifications, allowing for further exploration of its biological activities and therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1095223-35-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,5,2,2 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1095223-35:
(9*1)+(8*0)+(7*9)+(6*5)+(5*2)+(4*2)+(3*3)+(2*3)+(1*5)=140
140 % 10 = 0
So 1095223-35-0 is a valid CAS Registry Number.
1095223-35-0Relevant articles and documents
Expedient synthesis of 3-alkoxymethyl- And 3-aminomethyl-pyrazolo[3,4-b] pyridines
Beutner, Gregory L.,Kuethe, Jeffrey T.,Kim, Mary M.,Yasuda, Nobuyoshi
supporting information; experimental part, p. 789 - 794 (2009/06/20)
An effective strategy has been developed for the preparation of 3-alkoxymethyl-pyrazolo[3,4-b]pyridines, compounds that are currently not readily accessible by existing synthetic methods. Further manipulation of these compounds allows for access to 3-alkoxymethyl-pyrazolo[3,4-b]pyridines with a variety of substitution patterns as well as 3-aminomethyl-pyrazolo[3,4-b] pyridines.
