13322-19-5 Usage
Description
(5-METHYL-2-PHENYL-2H-1,2,3-TRIAZOL-4-YL)METHANOL, a triazole derivative with the molecular formula C10H11N3O, is a chemical compound that features a phenyl and a methyl group attached to a triazole ring, along with a hydroxyl group. Known for its pharmacological activities, this compound is a promising molecule in medicinal chemistry and drug development due to the diverse properties of the triazole ring system.
Uses
Used in Pharmaceutical Industry:
(5-METHYL-2-PHENYL-2H-1,2,3-TRIAZOL-4-YL)METHANOL is used as a building block for the synthesis of various pharmaceutical compounds, owing to its versatile hydroxyl group that allows for the creation of a wide range of drug molecules.
Used in Medicinal Chemistry Research:
(5-METHYL-2-PHENYL-2H-1,2,3-TRIAZOL-4-YL)METHANOL is utilized as a key component in the development of new drugs, given its potential antimicrobial, antifungal, and anticancer properties, which are valuable for research and development in the pharmaceutical sector.
Used in Drug Development:
(5-METHYL-2-PHENYL-2H-1,2,3-TRIAZOL-4-YL)METHANOL is employed as a precursor in the formulation of new therapeutic agents, capitalizing on the pharmacological activities associated with the triazole ring system to address various medical conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 13322-19-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,2 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13322-19:
(7*1)+(6*3)+(5*3)+(4*2)+(3*2)+(2*1)+(1*9)=65
65 % 10 = 5
So 13322-19-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H11N3O/c1-8-10(7-14)12-13(11-8)9-5-3-2-4-6-9/h2-6,14H,7H2,1H3
13322-19-5Relevant articles and documents
PYRAZOLE DERIVATIVES
-
Page/Page column 50, (2010/10/19)
A compound represented by the general formula (I), which is useful as a peroxisome proliferator-activated receptor α/γ agonist, a salt of the compound, and a solvate of either. (In the formula, X, Y, and Z each represents nitrogen or carbon; m is an integ
Reaction of 2-phenyl substituted 1,2,3-triazol 1-oxides with acylating agents. Preparation of hydroxy- halogen- hydroxymethyl- and chloromethyltriazoles
Begtrup, Mikael
, p. 717 - 728 (2007/10/03)
2-Phenyltriazol 1-oxides react with acetyl chloride producing acetoxy- and chloro-substituted triazoles.The substituents enter the 5 and the 4-position.When these are not accessible the substituents go to lateral positions and to the phenyl group producing acetoxymethyltriazoles and 2-halogenophenyl triazoles.Acetic anhydride reacts reluctantly while trifluoroacetic anhydride is more reactive producing trifluoroacetoxytriazoles.The reactions provide effective routes to hydroxy- and hydroxymethyltriazoles.Several mechanisms among which a cyclic one are operating.
