1-Acetyl-1H-1,2,3-triazolo[4,5-b]pyridine TCI A1219

Chemical Identity

CAS No.: 107866-54-6
PubChem: CID 702889·SID 87562689
Formula: C7H6N4O
Molecular weight: 162.15 g/mol
Purity: >98.0%(T)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 1-(triazolo[4,5-b]pyridin-1-yl)ethanone
SMILES: CC(=O)N1C2=C(N=CC=C2)N=N1
InChIKey: SDYATKOQVBKTLQ-UHFFFAOYSA-N

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1-Acetyl-1H-1,2,3-triazolo[4,5-b]pyridine is a synthetic chemical compound widely used in laboratory settings for its versatility in organic synthesis. This compound plays a key role in various chemical reactions, particularly in the fields of protection, deprotection, and derivatization. Its unique molecular structure allows it to participate in a range of reactions, including substitution, coupling, and molecular modification. Due to its reactivity and functional group compatibility, it is a valuable tool for chemists working on complex molecule synthesis.

The compound is known for its chemical stability under controlled conditions, making it reliable for use in laboratory experiments. However, it is sensitive to moisture and light exposure, which requires careful handling and storage. Its high reactivity and selectivity make it a preferred choice for applications requiring precise chemical transformations. The compound’s ability to interact with different functional groups enhances its utility in both academic and industrial research environments.

In Indonesian laboratories, 1-Acetyl-1H-1,2,3-triazolo[4,5-b]pyridine is commonly used in organic chemistry research, especially in the development of new compounds and molecular modifications. It is also employed in pharmacological studies and drug synthesis due to its capacity to participate in complex chemical reactions that yield bioactive compounds. Its availability in various packaging options ensures convenience for both small-scale and large-scale experimental needs.

TCI brochures (PDF)

Protecting Agents 2025-03-25 · p. 7

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Organic synthesis is a key application where this compound is used to facilitate complex molecular transformations due to its reactivity and functional group compatibility.
Drug development benefits from its ability to participate in reactions that yield bioactive compounds, supporting pharmaceutical research in Indonesia.
Functional group modification is enhanced by its participation in deprotection and derivatization processes, making it ideal for advanced chemical synthesis.
Analytical chemistry applications leverage its reactivity for molecular characterization and structural analysis in laboratory settings.
Research in medicinal chemistry relies on its unique structure to enable the synthesis of compounds with specific biological activities.

Brand	TCI
CAS number	107866-54-6
Molecular formula	—
Purity	—
Category	Chemistry > Synthetic Reagents > Protection, Deprotection, Derivatization
Pack sizes	Available in various packaging options for different experimental scales
Physical form	Solid, typically in powder or crystalline form
Storage	Store in a cool, dry place away from moisture and direct light

This compound should be stored in a cool, dry environment to prevent degradation due to moisture and light exposure. It is recommended to use airtight containers made of glass or high-density polyethylene to maintain its stability. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to avoid prolonged exposure to air and to ensure that storage conditions are consistent with the compound’s sensitivity. Proper labeling and storage practices help minimize risks and ensure safe usage in laboratory environments.

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