Ethyl 2-(2-Benzothiazolyl)acetate TCI B2168

Chemical Identity

CAS No.: 29182-42-1
PubChem: CID 359796·SID 87565030
Formula: C11H11NO2S
Molecular weight: 221.28 g/mol
Purity: >95.0%(HPLC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: ethyl 2-(1,3-benzothiazol-2-yl)acetate
SMILES: CCOC(=O)CC1=NC2=CC=CC=C2S1
InChIKey: VYMJUZXFYAREJY-UHFFFAOYSA-N

Rp 1.749.300,00

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Ethyl 2-(2-Benzothiazolyl)acetate is a chemical compound widely used as a building block in the synthesis of heterocyclic compounds. This material plays a crucial role in laboratory settings where the development of complex molecular structures is required. Its unique molecular structure, featuring a benzothiazole group attached to an acetic acid chain, makes it an essential component in the creation of various bioactive molecules. Due to its versatility and chemical stability, it is frequently employed in research aimed at discovering new pharmaceuticals and advanced materials.

One of the key properties that make Ethyl 2-(2-Benzothiazolyl)acetate a preferred choice is its controlled reactivity and compatibility with a wide range of functional groups. This allows chemists to modify the molecule efficiently during synthetic processes. Additionally, its solubility in organic solvents simplifies purification and isolation steps, making it a practical option for laboratory work. These characteristics contribute to its popularity in both academic and industrial research environments.

In Indonesian laboratories, Ethyl 2-(2-Benzothiazolyl)acetate is commonly used in pharmaceutical and organic chemistry research. It is integral to studies focused on drug development and the synthesis of heterocyclic compounds. Many research institutions and universities rely on this compound for its reliability and effectiveness in chemical reactions, supporting ongoing scientific advancements in the region.

Related TCI products

Pharmaceutical research utilizes Ethyl 2-(2-Benzothiazolyl)acetate for the synthesis of bioactive compounds due to its structural versatility and reactivity.
Organic chemistry experiments benefit from its solubility in organic solvents, facilitating efficient purification and reaction processes.
Drug discovery projects incorporate this compound to develop new therapeutic agents with targeted biological activities.
Material science studies use it to create advanced polymers and functional materials with unique chemical properties.
Academic research institutions rely on it for teaching and experimental purposes in heterocyclic chemistry courses.

Brand	TCI
CAS number	29182-42-1
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes	—
Physical form	—
Storage	Store in a cool, dry place away from light and incompatible materials

Ethyl 2-(2-Benzothiazolyl)acetate should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a sealed container to prevent exposure to moisture and air. Due to its organic nature, it should be stored away from strong oxidizers and reactive materials to avoid potential chemical interactions. Laboratory personnel should handle the compound with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safe handling. Regular monitoring of storage conditions is essential to maintain the integrity of the compound and ensure its usability in research applications.

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