3-Thiophenecarboxaldehyde TCI T0864

Chemical Identity

CAS No.: 498-62-4
PubChem: CID 68135·SID 87576693
Formula: C5H4OS
Molecular weight: 112.15 g/mol
Purity: >98.0%(GC)
Reference databases: ChEBI·ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: thiophene-3-carbaldehyde
SMILES: C1=CSC=C1C=O
InChIKey: RBIGKSZIQCTIJF-UHFFFAOYSA-N

Rp 1.405.950,00

~~Rp 998.550,00~~ Rp 1.405.950,00

Sale Sold out

Shipping calculated at checkout.

Berat 5g 25g

Pembayaran hanya melalui request quotation dan dilakukan setelah tim kami menghubungi Anda. Mohon cantumkan nomor WhatsApp aktif untuk konfirmasi pesanan & pembuatan invoice. Estimasi pengiriman 2-4 minggu setelah pembayaran.

Dokumen Keamanan & Mutu

↓ Unduh SDS / MSDS (PDF resmi TCI)

CoA (Certificate of Analysis)

Spesifik per batch produksi — diterbitkan dan dikirim bersama barang sesuai nomor lot yang Anda terima.

Contoh CoA segera tersedia.

💬 Minta CoA via WhatsApp

View full details

3-Thiophenecarboxaldehyde is a chemical compound widely used in laboratory settings for the synthesis of heterocyclic compounds and complex organic molecules. As a key building block in chemical research, it serves as a fundamental component in the development of various chemical structures. Its versatility makes it an essential reagent for chemists working on diverse synthetic pathways. This compound is particularly valuable for its ability to participate in multiple reaction types, making it a go-to material for advanced chemical experimentation.

The unique chemical structure of 3-Thiophenecarboxaldehyde, featuring a thiophene ring and an aldehyde group, contributes to its high reactivity. This reactivity allows it to engage in reactions such as condensation, substitution, and coupling with other organic compounds. Its chemical properties make it highly suitable for the synthesis of bioactive molecules and functional materials. The presence of the aldehyde group also enables it to react with a variety of reagents, enhancing its utility in organic synthesis.

In Indonesian laboratories, 3-Thiophenecarboxaldehyde is extensively used in organic chemistry research, especially in the development of new compounds with potential applications in pharmaceuticals, materials science, and chemical industries. Its relevance in research that requires the synthesis of heterocyclic structures makes it a critical reagent for both academic and industrial chemical studies.

TCI brochures (PDF)

Thiophenes 2026-06-29 · p. 8

Related TCI products

Organic synthesis of heterocyclic compounds due to its reactive aldehyde group and thiophene ring.
Development of bioactive molecules for pharmaceutical research as a versatile building block.
Synthesis of functional materials in material science applications for its structural versatility.
Use in academic research for teaching and experimental purposes in chemistry laboratories.
Support for industrial chemical processes requiring the production of complex organic structures.

Brand	TCI
CAS number	498-62-4
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid or liquid depending on the specific product variant
Storage	Store in a cool, dry place away from moisture and direct sunlight

3-Thiophenecarboxaldehyde should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to moisture and air, which could lead to degradation. Due to its reactivity, it should be handled in a well-ventilated area, and appropriate personal protective equipment should be worn. Avoid contact with incompatible substances such as strong oxidizers. Keep the material away from heat sources and ensure proper labeling for safe handling and storage in laboratory settings.

—