1031750-29-4 Usage
General Description
3H-Imidazo[4,5-c]pyridin-4-amine, 7-methyl- is a chemical compound that belongs to the class of imidazo[4,5-c]pyridine derivatives. It is characterized by the presence of a 7-methyl group on the imidazopyridine core structure. 3H-Imidazo[4,5-c]pyridin-4-amine, 7-methyl- has potential pharmaceutical significance as it can interact with biological targets and modulate their function. It may have applications in medicinal chemistry and drug discovery research for the development of new therapeutic agents. Additionally, 3H-Imidazo[4,5-c]pyridin-4-amine, 7-methyl- may be of interest in the study of structure-activity relationships and pharmacological properties of imidazopyridine derivatives.
Check Digit Verification of cas no
The CAS Registry Mumber 1031750-29-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,1,7,5 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1031750-29:
(9*1)+(8*0)+(7*3)+(6*1)+(5*7)+(4*5)+(3*0)+(2*2)+(1*9)=104
104 % 10 = 4
So 1031750-29-4 is a valid CAS Registry Number.
1031750-29-4Relevant articles and documents
Tetramethylsuccinimide as a directing/protecting group in purine glycosylates
Arico, Joseph W.,Calhoun, Amy K.,Salandria, Kerry J.,McLaughlin, Larry W.
supporting information; experimental part, p. 120 - 122 (2010/05/18)
Chemical Equation Presented Tetramethylsuccinic anhydride can be used to protect the exocyclic amine of 6-aminopurine derivatives by forming the corresponding tetramethysuccinimide. X-ray crystallography confirms that the imide carbonyl and the methyl groups are positioned to sterically block the N7 nitrogen so that glycosylations occur with very high regiochemical control at N9. This approach is particularly effective for 3-substituted purines where the substituent tends to block access to N9 and inhibit glycosylation at that site.
