58360-86-4 Usage
Uses
Used in Pharmaceutical Research:
N-benzyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine is used as a potential drug candidate for the treatment of various diseases, leveraging its anti-inflammatory, antiviral, and anticancer properties. Its unique chemical structure and therapeutic potential make it a valuable asset in the development of new medications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, N-benzyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine is employed for the synthesis of novel compounds with improved pharmacological profiles. Its versatile structure allows for modifications to enhance its therapeutic effects and reduce potential side effects, contributing to the advancement of drug discovery.
Used in Drug Development:
N-benzyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine is utilized in drug development to explore its potential applications in treating a range of diseases. Ongoing research and development efforts aim to optimize its properties and evaluate its safety and efficacy, with the goal of bringing new therapeutic options to patients in need.
Used in Anticancer Applications:
As an anticancer agent, N-benzyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine is used to target and inhibit the growth of cancer cells. Its potential to modulate various oncological signaling pathways and exert inhibitory effects on tumor growth and progression makes it a promising candidate for cancer treatment.
Used in Antiviral Applications:
In antiviral applications, N-benzyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine is employed to combat viral infections by inhibiting viral replication and reducing the severity of symptoms. Its antiviral properties make it a valuable tool in the development of new antiviral therapies.
Used in Anti-inflammatory Applications:
N-benzyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine is used as an anti-inflammatory agent to reduce inflammation and alleviate symptoms associated with various inflammatory conditions. Its potential to modulate inflammatory pathways and provide relief from inflammation-related discomfort positions it as a promising option for inflammatory disease management.
Check Digit Verification of cas no
The CAS Registry Mumber 58360-86-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,3,6 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 58360-86:
(7*5)+(6*8)+(5*3)+(4*6)+(3*0)+(2*8)+(1*6)=144
144 % 10 = 4
So 58360-86-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H11N5/c1-2-4-9(5-3-1)6-13-11-10-7-16-17-12(10)15-8-14-11/h1-5,7-8H,6H2,(H2,13,14,15,16,17)
58360-86-4Relevant academic research and scientific papers
A microwave-assisted SmI2-catalyzed direct N-alkylation of anilines with alcohols
Gour, Jitendra,Gatadi, Srikanth,Malasala, Satyaveni,Yaddanpudi, Madhavi Venkata,Nanduri, Srinivas
, p. 7488 - 7494 (2019/06/14)
A new protocol for the alkylation of aromatic amines has been described using alcohols in the presence of SmI2 as a catalyst with the generation of water as the sole byproduct. The reaction proceeds under MW conditions and selectively generates monoalkylated amines. This protocol features a broad substrate scope and good functional-group tolerance with moderate to high yields.
