13322-19-5 Usage
General Description
(5-Methyl-2-phenyl-2H-1,2,3-triazol-4-yl)methanol is a chemical compound with the molecular formula C10H11N3O. It is a triazole derivative that contains a phenyl and a methyl group, as well as a hydroxyl group. (5-METHYL-2-PHENYL-2H-1,2,3-TRIAZOL-4-YL)METHANOL has potential applications in medicinal chemistry and drug development, as triazoles are known for their pharmacological activities. The presence of a hydroxyl group makes it a versatile building block for the synthesis of various pharmaceutical compounds. Additionally, the triazole ring system in this compound has been found to have antimicrobial, antifungal, and anticancer properties, making it a valuable molecule for research and development in the pharmaceutical industry.
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
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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.
