3912-22-9 Usage
Structure
1H-1,2,3-Triazole-1-acetic acid, 4-(hydroxymethyl)-, ethyl ester is a heterocyclic organic compound with a triazole ring fused to an acetic acid group and an ethyl ester group attached to the 4-position of the hydroxymethyl group.
Functional groups
Triazole ring, acetic acid group, hydroxymethyl group, and ethyl ester group.
Appearance
It is likely a colorless or pale-colored solid or liquid, depending on the conditions.
Solubility
It is expected to be soluble in polar solvents such as water, methanol, and ethanol due to the presence of the hydroxymethyl and ethyl ester groups.
Stability
The compound may be sensitive to heat, light, and moisture, as it contains a triazole ring and ester functional groups.
Reactivity
It may react with strong acids, strong bases, and nucleophiles due to the presence of the ester functional group.
Potential applications
Pharmaceutical industry, agrochemicals, and materials science.
Safety precautions
Handle with care and follow all safety guidelines, as with any chemical substance.
Storage
Store in a cool, dry, and well-ventilated area, away from heat, light, and moisture, in a sealed container.
Check Digit Verification of cas no
The CAS Registry Mumber 3912-22-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,1 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3912-22:
(6*3)+(5*9)+(4*1)+(3*2)+(2*2)+(1*2)=79
79 % 10 = 9
So 3912-22-9 is a valid CAS Registry Number.
3912-22-9Relevant articles and documents
Pyridinyl-triazole ligand systems for highly efficient CuI-catalyzed azide-alkyne cycloaddition
Chen, Yunfeng,Meng, Xianggao,Wang, Ye,Zheng, Lei
, (2020/10/02)
Pyridinyl-triazole ligand systems (including N2-2-pyridinyl 1,2,3-triazoles and N1/N2-substituted 2-(NH-1,2,3-triazol-4-yl)pyridines) were found to be superior ligands for CuI-catalyzed azide-alkyne cycloaddition (CuAAC) r
Some Aspects of the Azide-Alkyne 1,3-Dipolar Cycloaddition Reaction
Pokhodylo,Tupychak,Shyyka, O. Ya.,Obushak
, p. 1310 - 1321 (2019/11/03)
Some peculiar features of two most commonly used catalytic systems (Cul and CuSOVsodium ascorbate) controlling the regioselectivity of 1,3-dipolar cycloaddition of azides to terminal alkynes have been studied. Their potentialities, main disadvantages, and limitations have been demonstrated by a number of examples, including reactions of low-molecular-weight azides and alkynes containing heterocyclic substituents. The possibility of using novel reagents in click reactions is discussed.
Harnessing the Dual Properties of Thiol-Grafted Cellulose Paper for Click Reactions: A Powerful Reducing Agent and Adsorbent for Cu
Rull-Barrull, Jordi,d'Halluin, Martin,Le Grognec, Erwan,Felpin, Fran?ois -Xavier
supporting information, p. 13549 - 13552 (2016/10/21)
A new approach exploiting the dual properties of thiol-grafted cellulose paper for promoting copper-catalyzed [3+2]-cycloadditions of organic azides with alkynes and adsorbing residual copper species in solution was developed. The thiol-grafted cellulose
