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Catalog Number:
17164
CAS Number:
6639-57-2
1,3-Benzotiazol-2-carbaldehído
Purity:
≥ 95% (RMN)
Synonym(s):
Benzotiazol-2-carbaldehído
Documents
$43.87 /1G
Tamaño
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Product Information

1,3-Benzothiazole-2-carbaldehyde is a versatile compound widely recognized for its applications in the fields of organic synthesis and pharmaceuticals. This aromatic aldehyde is characterized by its unique benzothiazole structure, which enhances its reactivity and makes it an essential building block in the synthesis of various heterocyclic compounds. Researchers often utilize 1,3-benzothiazole-2-carbaldehyde in the development of agrochemicals, dyes, and pharmaceuticals, particularly in the synthesis of biologically active molecules. Its ability to act as a precursor in the formation of thiazole derivatives further underscores its significance in medicinal chemistry, where it has been explored for potential anti-cancer and anti-inflammatory properties.

The compound's distinctive properties, such as its moderate solubility in organic solvents and stability under standard laboratory conditions, make it an attractive choice for both academic and industrial applications. Additionally, its relatively simple synthesis route allows for easy incorporation into complex molecular architectures, providing researchers with a valuable tool for the development of innovative chemical products. With its broad range of applications and potential for new discoveries, 1,3-benzothiazole-2-carbaldehyde stands out as a key compound for professionals in the chemical and pharmaceutical industries.

Synonyms
Benzotiazol-2-carbaldehído
CAS Number
6639-57-2
Purity
≥ 95% (RMN)
Molecular Formula
C8H5NOS
Molecular Weight
163.2
MDL Number
MFCD00526215
PubChem ID
241608
Appearance
Naranja sólido
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Benzotiazol-2-carbaldehído
CAS Number
6639-57-2
Purity
≥ 95% (RMN)
Molecular Formula
C8H5NOS
Molecular Weight
163.2
MDL Number
MFCD00526215
PubChem ID
241608
Appearance
Naranja sólido
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

1,3-Benzothiazole-2-carbaldehyde is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-cancer and anti-inflammatory drugs, enhancing therapeutic options.
  • Fluorescent Dyes: It is used in the production of fluorescent dyes, which are essential in biological imaging and diagnostics, allowing researchers to visualize cellular processes with high precision.
  • Agricultural Chemicals: The compound plays a role in formulating agrochemicals, including pesticides and fungicides, providing effective solutions for crop protection and improving agricultural yields.
  • Material Science: It is incorporated into the development of advanced materials, such as polymers and coatings, which exhibit enhanced durability and chemical resistance, benefiting industries like automotive and construction.
  • Analytical Chemistry: This chemical is utilized in various analytical techniques, including chromatography and spectroscopy, aiding in the detection and quantification of other substances in complex mixtures.

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