CAS 4701-17-1

5-Bromo-2-tiofenocarboxaldeído

Descrição:

5-Bromo-2-tiofenocarboxaldeído é um composto orgânico caracterizado pela presença de um átomo de bromo e um anel de tiofeno, que é um heterociclo aromático de cinco membros contendo enxofre. Este composto apresenta um grupo funcional carboxaldeído (-CHO) ligado ao anel de tiofeno, especificamente na posição 2, e um substituinte de bromo na posição 5. A presença do átomo de bromo aumenta a reatividade do composto, tornando-o útil em várias aplicações sintéticas, incluindo a preparação de moléculas orgânicas mais complexas. O anel de tiofeno contribui para a aromaticidade do composto, influenciando suas propriedades eletrônicas e estabilidade. 5-Bromo-2-tiofenocarboxaldeído é tipicamente usado em síntese orgânica, particularmente no desenvolvimento de produtos farmacêuticos e agroquímicos. Sua estrutura única permite aplicações potenciais em ciência dos materiais e como um bloco de construção na síntese de derivados de tiofeno funcionalizados. Assim como muitos compostos orgânicos, o manuseio deve ser feito com cuidado, considerando os protocolos de segurança devido à potencial toxicidade e reatividade.

Fórmula: C₅H₃BrOS

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

Chave InChI: InChIKey=GFBVUFQNHLUCPX-UHFFFAOYSA-N

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

Sinónimos:

• 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

Fórmula: C₅H₃BrOS

Pureza: >97.0%(GC)

Cor e Forma: White or Colorless to Yellow to Orange powder to lump to clear liquid

Peso molecular: 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

Fórmula: C₅H₃BrOS

Pureza: 97%

Cor e Forma: Clear, pale yellow to yellow to orange or brown to dark brown, Liquid

Peso molecular: 191.04

Ref: 02-A13381

5-Bromo-2-thiophenecarboxaldehyde

CAS: 4701-17-1

Fórmula: C₅H₃BrOS

Pureza: 97%

Cor e Forma: Solid

Peso molecular: 191.0457

Ref: IN-DA0037UQ

5-Bromothiophene-2-carboxaldehyde

CAS: 4701-17-1

Fórmula: C₅H₃BrOS

Peso molecular: 191.05

Ref: 7W-GK5567

5-Bromothiophene-2-carboxaldehyde

CAS: 4701-17-1

5-Bromothiophene-2-carboxaldehyde

Fórmula: C₅H₃BrOS

Pureza: 97%

Cor e Forma: dark brown to dark beige with solid particles liquid

Peso molecular: 191.05g/mol

Ref: 54-OR18347

5-Bromo-2-thiophenecarboxaldehyde

Produto Controlado

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);

Fórmula: C₅H₃BrOS

Cor e Forma: Neat

Peso molecular: 191.05

Ref: TR-B688130

5-Bromothiophene-2-carbaldehyde

CAS: 4701-17-1

Fórmula: C₅H₃BrOS

Pureza: 97%

Cor e Forma: Clear

Peso molecular: 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.

Fórmula: C₅H₃BrOS

Pureza: Min. 95%

Cor e Forma: Yellow Powder

Peso molecular: 191.05 g/mol

Ref: 3D-FB12607