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1H-1,2,3-Triazole

ALDRICH/333662 - 97%

Synonym: 2,3-Diazapyrrole; 2H-1,2,3-Triazole; Osotriazole; Pyrrodiazole; Triazacyclopentadiene

CAS Number: 288-36-8
Empirical Formula (Hill Notation): C2H3N3
Molecular Weight: 69.07
MDL Number: MFCD00014490
Linear Formula: C2H3N3
Product Type: Chemical
Catalog Number PKG Qty. Price Quantity
45-333662-1G 1 g
 $56.50
1/EA		 Add To Favorites
45-333662-5G 5 g
 $154.00
1/EA		 Add To Favorites

 

assay 97%
bp 203 °C/752 mmHg (lit.)
density 1.192 g/mL at 25 °C (lit.)
form liquid
InChI 1S/C2H3N3/c1-2-4-5-3-1/h1-2H,(H,3,4,5)
InChI key QWENRTYMTSOGBR-UHFFFAOYSA-N
mp 23-25 °C (lit.)
refractive index n20/D 1.498 (lit.)
SMILES string c1c[nH]nn1
Application: • Crystalline framework materials: Research on triazole carboxylic acid ligand has demonstrated its application in smart crystalline framework materials, notably for fluorescence sensing and catalytic reduction of p-nitrophenol, illustrating its utility in chemical sensing and environmental applications (Lv et al., 2023 ).
• PXR receptor modulation: 1H-1,2,3-Triazole-4-carboxamides have been optimized as potent and selective inverse agonists and antagonists of the PXR receptor, providing insights into the design of receptor-specific drugs (Li et al., 2022 ).
• Large-scale synthesis: The large-scale synthesis of a Notum inhibitor employing a modified Sakai reaction illustrates the importance of 1H-1,2,3-triazole in the production of biochemical reagents, which can be essential in medical research and drug development (Atkinson et al., 2022 ).
General description: 2H-1,2,3-triazole is tautomeric form of 1H-1,2,3-triazole. 1H-1,2,3-triazole effectively promotes the proton conduction in polymer electrolyte membranes via an intermolecular proton-transfer mechanism.
Packaging: 1, 5 g in glass bottle
Purity 97%
bp 203 °C/752 mmHg (lit.)
mp 23-25 °C (lit.)
Density 1.192 g/mL at 25 °C (lit.)
Refractive Index n20/D 1.498 (lit.)
UNSPSC 12352100

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