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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)-

1H-Pyrrole-2-carboxaldehyde, 5-methyl-

Cc1ccc([nH]1)C=O Request for Quotation
Chemical Name: 1H-Pyrrole-2-carboxaldehyde, 5-methyl-
CAS Number: 1192-79-6
Product Number: AG000IC8(AGN-PC-0JKBS0)
Synonyms:
MDL No:
Molecular Formula: C6H7NO
Molecular Weight: 109.1259

Identification/Properties

Properties
BP:
226.1°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
109.128g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
109.053g/mol
Monoisotopic Mass:
109.053g/mol
Topological Polar Surface Area:
32.9A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
92.5
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H319
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Methylpyrrole-2-carbaldehyde is a versatile chemical compound that finds crucial applications in various chemical synthesis processes. This compound serves as a key building block in the creation of pharmaceuticals, agrochemicals, and materials science. Its unique structure and reactivity make it a valuable reagent for the synthesis of complex organic molecules.In chemical synthesis, 5-Methylpyrrole-2-carbaldehyde is commonly utilized as a starting material for the preparation of heterocyclic compounds. By undergoing various transformations and reactions, this compound can be used to introduce functional groups, such as alcohols, amines, and carboxylic acids, into the final product. Additionally, its ability to participate in multiple types of reactions, such as condensation, oxidation, and reduction, further expands its utility in synthesis pathways.Furthermore, 5-Methylpyrrole-2-carbaldehyde plays a significant role in the development of new drug molecules. Its presence in the molecular structure of pharmaceutical compounds can impart desired biological activities, making it a valuable intermediate in medicinal chemistry. By incorporating this compound into drug design strategies, chemists can modulate the pharmacological properties of potential therapeutic agents.Overall, the application of 5-Methylpyrrole-2-carbaldehyde in chemical synthesis enables researchers to access diverse chemical space and construct complex molecular architectures efficiently and strategically. Its role as a key intermediate highlights its importance in advancing the field of organic chemistry and driving innovation in various sectors of the chemical industry.