274-71-5 Usage
Description
Pyrazolo[1,5-a]pyrimidine is a light yellow solid with unique chemical properties that make it a subject of interest in various research fields. It is a heterocyclic compound characterized by its specific molecular structure, which includes a pyrazolo and a pyrimidine ring fused together.
Uses
Used in Pharmaceutical Industry:
Pyrazolo[1,5-a]pyrimidine is used as a protein kinase CK2 inhibitor for its potential role in the development of novel therapeutics. Protein kinase CK2 is an enzyme that plays a crucial role in various cellular processes, and its dysregulation has been implicated in several diseases, including cancer. By inhibiting this enzyme, Pyrazolo[1,5-a]pyrimidine may help in the development of targeted treatments for these conditions.
Additionally, due to its unique chemical structure, Pyrazolo[1,5-a]pyrimidine may also have potential applications in other areas of the pharmaceutical industry, such as the development of new drugs for other diseases or as a building block for the synthesis of more complex molecules with specific biological activities. However, further research is needed to fully understand its potential and limitations in these areas.
Check Digit Verification of cas no
The CAS Registry Mumber 274-71-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,7 and 4 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 274-71:
(5*2)+(4*7)+(3*4)+(2*7)+(1*1)=65
65 % 10 = 5
So 274-71-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H5N3/c1-3-7-6-2-4-8-9(6)5-1/h1-5H
274-71-5Relevant articles and documents
Studies with functionally substituted enamines: The reactivity of enaminals and enamino esters toward naphthoquinone, hydrazonoyl halides, aminoazoles and hippuric acid
Al-Saleh, Balkis,Makhseed, Saad,Hassaneen, Huwaida M. E.,Elnagdi, Mohamed Hilmy
, p. 59 - 62 (2006)
Whereas enamines 1a,b react with naphthoquinone (2) to yield the naphthofuranals 5a,b, enamine ester 1c react with 2 to yield benzoindole derivatives 7. Enamine 1b reacts with hydrazonoyl halides 8 to yield 3,4-disubstituted pyrazoles 12. On the other hand, the enaminal 1a failed to react with 8, while enamine ester 1c afforded hydrazone 16 on treatment with 8. The enamino ester 1b afforded triethyl 1,3,5-benzenetricarboxylates on refluxing in acetic acid. Georg Thieme Verlag Stuttgart.
N- and O-substituted aminophenols, method and use for diagnosis
-
, (2008/06/13)
The present invention provides N- and O-substituted aminophenol derivatives of the general formula STR1 wherein R1, R2, R3, G and L are as hereinbefore defined. The present invention also provides intermediates for the preparation of these aminophenol derivatives of general formula (I), as well as the use of the aminophenol derivatives of general formula (I) for the determination of hydrolyses, as well as for the preparation of agents for carrying out determinations of hydrolyses.
