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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)-

2-propan-2-ylpyrimidine-4-carbaldehyde

O=Cc1ccnc(n1)C(C)C Request for Quotation
Chemical Name: 2-propan-2-ylpyrimidine-4-carbaldehyde
CAS Number: 944901-13-7
Product Number: AG006AB7(AGN-PC-05BJ2C)
Synonyms:
MDL No:
Molecular Formula: C8H10N2O
Molecular Weight: 150.1778

Identification/Properties

Properties
BP:
230.0±13.0 °C(Predicted)
Computed Properties
Molecular Weight:
150.181g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
150.079g/mol
Monoisotopic Mass:
150.079g/mol
Topological Polar Surface Area:
42.8A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
136
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Isopropylpyrimidine-4-carbaldehyde is a versatile chemical compound commonly utilized in chemical synthesis processes. As a key intermediate in the production of various pharmaceuticals and agrochemicals, this compound's unique structural properties make it an essential building block in the creation of a wide range of complex molecules. Thanks to its functional groups and reactivity, 2-Isopropylpyrimidine-4-carbaldehyde serves as a valuable tool in the development of innovative drugs, crop protection agents, and other biologically active substances. Its ability to undergo various chemical reactions, such as condensation, alkylation, and reduction, enables it to be tailored for specific synthetic pathways, providing chemists with a crucial component for creating diverse and beneficial products. This compound's significance in chemical synthesis lies in its capacity to facilitate the efficient and controlled construction of intricate molecular structures, advancing the fields of medicine, agriculture, and materials science.