Benzo[b]thiophene-2-carbonyl Chloride TCI B4637

Chemical Identity

CAS No.: 39827-11-7
PubChem: CID 142384·SID 253660619
Formula: C9H5ClOS
Molecular weight: 196.65 g/mol
Purity: >98.0%(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 1-benzothiophene-2-carbonyl chloride
SMILES: C1=CC=C2C(=C1)C=C(S2)C(=O)Cl
InChIKey: DNGLRCHMGDDHNC-UHFFFAOYSA-N

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Benzo[b]thiophene-2-carbonyl Chloride is a chemical compound widely used in laboratory settings as a building block for the synthesis of complex heterocyclic compounds. This compound contains a benzo[b]thiophene ring fused with a carbonyl chloride group, making it a versatile reagent in organic chemistry. Its structural complexity and reactivity make it a valuable tool for chemists working on the development of new pharmaceuticals and industrial chemicals. It is particularly useful in reactions that require the formation of new bonds through substitution or nucleophilic mechanisms.

The compound is known for its high reactivity and stability under controlled conditions, which makes it a preferred choice for various synthetic pathways. Its ability to participate in reactions such as Diels-Alder, acyl transfer, and electrophilic substitution highlights its importance in organic synthesis. The presence of the carbonyl chloride group allows for easy functionalization, enabling the creation of a wide range of derivatives. These properties make it a reliable and efficient reagent for advanced chemical research.

In Indonesian laboratories, Benzo[b]thiophene-2-carbonyl Chloride is commonly used in organic chemistry research, especially in pharmacology and the synthesis of bioactive compounds. Its availability through AMI Scientific ensures that researchers have access to this essential material for their experiments. The compound's role in creating complex molecular structures supports ongoing scientific advancements in both academic and industrial settings.

TCI brochures (PDF)

Thiophenes 2026-06-29 · p. 11
Building Blocks for Organic Semiconductor 2026-03-24 · p. 27

Related TCI products

Organic synthesis of heterocyclic compounds due to its reactive carbonyl chloride group and benzo[b]thiophene ring structure.
Development of pharmaceuticals and bioactive molecules through nucleophilic substitution and acyl transfer reactions.
Research in medicinal chemistry for the creation of compounds with specific biological activities and therapeutic potential.
Industrial chemical synthesis where complex molecular frameworks are required for the production of specialty chemicals.
Academic studies in organic chemistry focusing on the structural and functional properties of heterocyclic systems.

Brand	TCI
CAS number	39827-11-7
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities as per supplier specifications
Physical form	Solid or liquid, depending on supplier packaging
Storage	Store in a cool, dry place away from moisture and direct sunlight

Benzo[b]thiophene-2-carbonyl Chloride should be stored in a cool, dry place, away from moisture and direct sunlight to maintain its chemical integrity. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and degradation. Due to its reactivity, it should be handled in a well-ventilated area, preferably under a fume hood, to minimize exposure. Avoid contact with incompatible substances such as strong bases or reducing agents. Proper personal protective equipment, including gloves and safety goggles, should always be worn when handling this compound. Regular monitoring of storage conditions ensures the compound remains stable and suitable for use in laboratory applications.

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