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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)-

quinazoline-4-carbaldehyde

O=Cc1ncnc2c1cccc2 Request for Quotation
Chemical Name: quinazoline-4-carbaldehyde
CAS Number: 933747-26-3
Product Number: AG006G7F(AGN-PC-0ALR3A)
Synonyms:
MDL No:
Molecular Formula: C9H6N2O
Molecular Weight: 158.1567

Identification/Properties

Properties
BP:
324.093°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-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


Quinazoline-4-carbaldehyde serves as a versatile building block in chemical synthesis, playing a crucial role in the creation of various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure and reactivity make it a valuable precursor for the synthesis of a wide range of compounds. With its aromatic ring and aldehyde functional group, quinazoline-4-carbaldehyde can undergo various reactions, such as condensation, reduction, and substitution, allowing for the introduction of different functional groups and modifications to the molecular structure. This compound is particularly valuable in the development of new drug candidates, as it can be used as a key intermediate in the synthesis of potential therapeutic agents targeting various diseases. Its synthetic versatility and broad applicability make quinazoline-4-carbaldehyde an indispensable tool for organic chemists seeking to access diverse chemical space and create innovative molecular structures.