Benzo[b]thiophene-3-carboxaldehyde TCI B4086

Chemical Identity

CAS No.: 5381-20-4
PubChem: CID 227328·SID 253659762
Formula: C9H6OS
Molecular weight: 162.21 g/mol
Purity: >98.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 1-benzothiophene-3-carbaldehyde
SMILES: C1=CC=C2C(=C1)C(=CS2)C=O
InChIKey: WDJLPQCBTBZTRH-UHFFFAOYSA-N

Rp 1.113.000,00

~~Rp 793.800,00~~ Rp 1.113.000,00

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Benzo[b]thiophene-3-carboxaldehyde is a chemical compound widely used in organic reactions for the synthesis of complex heterocyclic compounds. This material serves as a crucial building block in laboratories that require foundational compounds for the formation of heterocyclic structures. Its presence in chemical laboratories highlights its importance in the development of compounds with diverse biological activities. The compound's molecular structure, featuring a benzo[b]thiophene ring containing sulfur, makes it a versatile reagent in synthetic chemistry.

The chemical and reactive properties of benzo[b]thiophene-3-carboxaldehyde make it an ideal choice for substitution and coupling reactions. Its ability to participate in various synthetic pathways enhances its utility in organic chemistry. The compound's reactivity and structural complexity contribute to its relevance in both academic and industrial research settings. It is particularly valuable in the synthesis of pharmaceutical compounds and other chemically complex molecules.

In Indonesian laboratories, benzo[b]thiophene-3-carboxaldehyde is commonly used in scientific research and educational settings to deepen understanding of molecular structures and heterocyclic reactivity. It plays a key role in drug development projects and the study of heterocyclic-based chemical compounds. Its application extends to both research and teaching, supporting advancements in chemical sciences and pharmaceutical innovation.

TCI brochures (PDF)

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

Related TCI products

Synthesis of complex heterocyclic compounds due to its structural versatility and reactivity in organic reactions.
Development of pharmaceutical compounds as a building block for creating bioactive molecules with therapeutic potential.
Educational use in chemical laboratories to teach students about heterocyclic structures and synthetic methodologies.
Research in medicinal chemistry for the design of new drugs and bioactive agents with targeted molecular interactions.
Exploration of chemical reactivity in laboratory settings to understand substitution and coupling mechanisms.

Brand	TCI
CAS number	5381-20-4
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes	As per supplier specifications
Physical form	Solid (as per standard product description)
Storage	Store in a cool, dry place away from light and moisture

Benzo[b]thiophene-3-carboxaldehyde should be stored in a cool, dry environment, away from direct light and moisture. It is recommended to use airtight containers to prevent exposure to air and humidity. As a chemical compound, it requires careful handling to avoid contamination and ensure stability. Laboratory personnel should wear appropriate personal protective equipment when handling the material. Proper storage conditions help maintain the compound's integrity and effectiveness in chemical reactions. Regular monitoring of storage conditions is essential to ensure long-term usability and safety in laboratory settings.

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