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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Benzaldehyde, 2-(1H-pyrrol-1-yl)-

O=Cc1ccccc1n1cccc1 Request for Quotation
Chemical Name: Benzaldehyde, 2-(1H-pyrrol-1-yl)-
CAS Number: 31739-56-7
Product Number: AG00BXK8(AGN-PC-0LK8ES)
Synonyms:
MDL No:
Molecular Formula: C11H9NO
Molecular Weight: 171.1953

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(1H-Pyrrol-1-yl)benzaldehyde, also known as benzaldehyde pyrrole, is a versatile organic compound widely utilized in chemical synthesis. This compound plays a crucial role in the field of organic chemistry due to its unique structural features and reactivity.One of the key applications of 2-(1H-Pyrrol-1-yl)benzaldehyde is its use as a building block in the synthesis of various heterocyclic compounds. Its aromatic ring and pyrrole moiety provide a valuable platform for the construction of complex organic molecules. By reacting with different nucleophiles and electrophiles, this compound can undergo a variety of transformations to yield diverse products with interesting properties.Furthermore, 2-(1H-Pyrrol-1-yl)benzaldehyde serves as a precursor for the synthesis of important pharmaceuticals and agrochemicals. Its ability to participate in multiple types of chemical reactions makes it a valuable intermediate in the production of bioactive compounds. Additionally, the presence of the pyrrole ring in its structure imparts specific biological activities to the synthesized molecules, making it a valuable tool in drug discovery and development.Overall, the versatile nature of 2-(1H-Pyrrol-1-yl)benzaldehyde makes it a valuable asset in the toolkit of organic chemists for the efficient synthesis of diverse compounds with potential applications in various industries.