CAS 4701-17-1

5-Bromo-2-thiophenecarboxaldehyde

Description:

5-Bromo-2-thiophenecarboxaldehyde is an organic compound characterized by the presence of a bromine atom and a thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. This compound features a carboxaldehyde functional group (-CHO) attached to the thiophene ring, specifically at the 2-position, and a bromine substituent at the 5-position. The presence of the bromine atom enhances the compound's reactivity, making it useful in various synthetic applications, including the preparation of more complex organic molecules. The thiophene ring contributes to the compound's aromaticity, influencing its electronic properties and stability. 5-Bromo-2-thiophenecarboxaldehyde is typically used in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its unique structure allows for potential applications in materials science and as a building block in the synthesis of functionalized thiophene derivatives. As with many organic compounds, handling should be done with care, considering safety protocols due to potential toxicity and reactivity.

Formula: C₅H₃BrOS

InChI: InChI=1/C5H3BrOS/c6-5-2-1-4(3-7)8-5/h1-3H

InChI key: InChIKey=GFBVUFQNHLUCPX-UHFFFAOYSA-N

SMILES: C(=O)C=1SC(Br)=CC1

Synonyms:

• 2-Bromo-5-formylthiophene
• 2-Bromo-5-thiophenecarboxaldehyde
• 2-Formyl-5-bromothiophene
• 2-Thiophenecarboxaldehyde, 5-bromo-
• 5-Bromo-2-carbonylthiophene
• 5-Bromo-2-formylthiophene
• 5-Bromo-2-thienylaldehyde
• 5-Bromo-2-thiophenaldehyde
• 5-Bromo-2-thiophenecarbaldehyde
• 5-Bromo-thiophene-2-carbaldehyde
• 5-Bromothiophen-2-carboxaldehyde
• 5-Bromothiophene-2-aldehyde
• 5-Bromothiophene-2-carbaldehyde
• 5-Bromothiophene-2-carboxaldehyde
• Labotest-Bb Lt00112291
• 5-Bromo-2-thiophenecarboxaldehyde
• TIMTEC-BB SBB000294
• AKOS BBS-00003268
• 2-BROMOTHIOPHENE-5-CARBOXALDEHYDE
• 5-BROMO-2-THIIOPHENE CARBOXALDEHYDE
• 5-BROMOTHIOPHENE-2-CARBALDEHYDE 98%
• 5-Bromothiophene-2-Aldehyde98%
• 5-Bromothiophene-2-Aldehyde 98%

5-Bromothiophene-2-carboxaldehyde

CAS: 4701-17-1

Formula: C₅H₃BrOS

Purity: >97.0%(GC)

Color and Shape: White or Colorless to Yellow to Orange powder to lump to clear liquid

Molecular weight: 191.04

Ref: 3B-B1135

5-Bromothiophene-2-carboxaldehyde, 97%

CAS: 4701-17-1

5-Bromo-2-thiophenecarboxaldehyde was used to prepare 5-[18F]fluoro-2-2-thiophene carboxaldehyde. Also is used in biological studies as anti-inflammatory and anti-tumor activity of the marine mangrove Rhizophora apiculata. This Thermo Scientific Chemicals brand product was originally part of the Al

Formula: C₅H₃BrOS

Purity: 97%

Color and Shape: Clear, pale yellow to yellow to orange or brown to dark brown, Liquid

Molecular weight: 191.04

Ref: 02-A13381

5-Bromothiophene-2-carboxaldehyde

CAS: 4701-17-1

5-Bromothiophene-2-carboxaldehyde

Formula: C₅H₃BrOS

Purity: 97%

Color and Shape: Liquid

Molecular weight: 191.04572

Ref: 54-OR18347

5-Bromo-2-thiophenecarboxaldehyde

CAS: 4701-17-1

Formula: C₅H₃BrOS

Purity: 98%

Color and Shape: Solid

Molecular weight: 191.0457

Ref: IN-DA0037UQ

5-Bromothiophene-2-carboxaldehyde

CAS: 4701-17-1

Formula: C₅H₃BrOS

Molecular weight: 191.05

Ref: 7W-GK5567

5-Bromothiophene-2-carbaldehyde

CAS: 4701-17-1

5-Bromothiophene-2-carbaldehyde

Formula: C₅H₃BrOS

Purity: 98% (stabilized with Cu+HQ+MgO)

Molecular weight: 191.05

Ref: IN-DG28791

5-Bromo-2-thiophenecarboxaldehyde

Controlled Product

CAS: 4701-17-1

Applications 5-Bromo-2-thiophenecarboxaldehyde is used in biological studies as anti-inflammatory and anti-tumor activity of the marine mangrove Rhizophora apiculata.
References Prabhu, V.V., et al.: J. Immunotoxicol., 9, 341 (2012);

Formula: C₅H₃BrOS

Color and Shape: Neat

Molecular weight: 191.05

Ref: TR-B688130

5-Bromothiophene-2-carbaldehyde

CAS: 4701-17-1

Formula: C₅H₃BrOS

Purity: 97%

Color and Shape: Clear

Molecular weight: 191.04

Ref: 10-F065250

5-Bromo thiophene-2-aldehyde

CAS: 4701-17-1

5-Bromo thiophene-2-aldehyde is a trifluoroacetic acid derivative used as an activatable probe for the study of biomolecular interactions. This compound has been shown to be biocompatible and has a low cytotoxicity. 5-Bromo thiophene-2-aldehyde binds to malonic acid in the presence of x-ray radiation and forms a complex that can be detected by electrochemical impedance spectroscopy. The structure of this complex was determined by x-ray crystal structures. This probe is also able to bind to nitrogen atoms in proteins, which can be used to diagnose cancer resistance through protease activity. 5-Bromo thiophene-2-aldehyde is isolated as its hydrochloride salt, which can be purified with a suzuki coupling reaction.

Formula: C₅H₃BrOS

Purity: Min. 95%

Color and Shape: Yellow Powder

Molecular weight: 191.05 g/mol

Ref: 3D-FB12607