CAS 881676-32-0

1H-Pyrrole-3-carboxaldehyde, 5-bromo-

Description:

1H-Pyrrole-3-carboxaldehyde, 5-bromo- is an organic compound characterized by its pyrrole ring structure, which is a five-membered aromatic heterocycle containing one nitrogen atom. The presence of a carboxaldehyde functional group at the 3-position contributes to its reactivity, allowing it to participate in various chemical reactions, such as nucleophilic additions and condensation reactions. The bromine substituent at the 5-position introduces additional reactivity and can influence the compound's electronic properties, making it useful in synthetic organic chemistry. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and form. It is soluble in organic solvents, which facilitates its use in various applications, including pharmaceuticals and agrochemicals. Safety precautions should be taken when handling this compound, as it may pose health risks, including irritation to the skin and eyes. Overall, 1H-Pyrrole-3-carboxaldehyde, 5-bromo- is a valuable building block in the synthesis of more complex organic molecules.

Formula: C₅H₄BrNO

Synonyms:

• 1H-Pyrrole-3-carbaldehyde,5-broMo-
• 1H-Pyrrole-3-carboxaldehyde, 5-broMo-
• 5-BroMo-1H-Pyrrole-3-carboxaldehyde
• 5-BroMo-1H-pyrrole-3-carbaldehyde

5-bromo-1h-pyrrole-3-carbaldehyde

CAS: 881676-32-0

Formula: C₅H₄BrNO

Purity: 96%

Color and Shape: Solid

Molecular weight: 173.9954

Ref: IN-DA0039J3

5-Bromo-1H-pyrrole-3-carbaldehyde

CAS: 881676-32-0

5-Bromo-1H-pyrrole-3-carbaldehyde

Purity: 98%

Molecular weight: 174.00g/mol

Ref: 54-OR93804

5-Bromo-1H-pyrrole-3-carbaldehyde

CAS: 881676-32-0

Formula: C₅H₄BrNO

Purity: 98%

Molecular weight: 173.997

Ref: 10-F383117

5-bromo-1H-pyrrole-3-carbaldehyde

CAS: 881676-32-0

5-bromo-1H-pyrrole-3-carbaldehyde is a phthalocyanine macrocycle that has been shown to be an excellent substrate for the synthesis of hydroporphyrins. This compound is systematically converted into brominated and chlorinated derivatives by treatment with elemental bromine or chlorine gas in the presence of a base. The cyclization reaction yields 2,6,10,14,18,22 tetrapyrroles. 5-Bromo-1H-pyrrole-3-carbaldehyde was synthesized from pyrrole and carbonyl bromide.

Formula: C₅H₄BrNO

Purity: Min. 95%

Molecular weight: 174 g/mol

Ref: 3D-GKB67632