96721-88-9 Usage
Description
4-(6-Aminopyridin-3-yl)phenol is a chemical compound with the molecular formula C11H10N2O. It is a derivative of phenol and contains a pyridine ring with an amino group attached at the 6th position. 4-(6-AMinopyridin-3-yl)phenol is known for its potential applications in various research and industrial fields.
Uses
Used in Pharmaceutical and Agrochemical Industries:
4-(6-Aminopyridin-3-yl)phenol is used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its unique structure allows it to be a key component in the development of new drugs and agricultural products.
Used in Neurological Disorder Research:
4-(6-Aminopyridin-3-yl)phenol is used as a potential treatment for neurological disorders. It has been studied for its ability to regulate certain neurotransmitter receptors in the brain, which could lead to advancements in the treatment of such conditions.
Used in Anti-Inflammatory and Antioxidant Research:
4-(6-AMinopyridin-3-yl)phenol is also being investigated for its potential anti-inflammatory and antioxidant properties. Its ability to modulate these biological processes could contribute to the development of new therapies for various inflammatory and oxidative stress-related diseases.
Further research is needed to fully understand the pharmacological and biological activities of 4-(6-Aminopyridin-3-yl)phenol, but its diverse potential applications highlight its importance in the scientific and medical fields.
Check Digit Verification of cas no
The CAS Registry Mumber 96721-88-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,7,2 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 96721-88:
(7*9)+(6*6)+(5*7)+(4*2)+(3*1)+(2*8)+(1*8)=169
169 % 10 = 9
So 96721-88-9 is a valid CAS Registry Number.
96721-88-9Relevant articles and documents
Synthesis and SAR studies of biaryloxy-substituted triazoles as antifungal agents
Liu, Ping,Zhu, Shaolong,Li, Peng,Xie, Weijie,Jin, Yongsheng,Sun, Qingyan,Wu, Qiuye,Sun, Peng,Zhang, Yingjun,Yang, Xiaohong,Jiang, Yuanying,Zhang, Dazhi
scheme or table, p. 3261 - 3265 (2009/04/06)
A series of 1-(substituted biaryloxy)-2-(2,4-difluorophenyl)-3-(1H-1,2,4-triazol-1-yl) propan-2-ol were synthesized and their antifungal activities were evaluated against eight human pathogenic fungi in vitro. Seventeen compounds showed activity 4- to 64-fold higher than voriconazole against Candida albicans. SAR clearly suggested that introduction of a biaryloxy side chain greatly enhanced the antifungal activity of triazole analogs against Candida species.
