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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-Cyclopropylpyrimidine-5-carbaldehyde

O=Cc1cnc(nc1)C1CC1 Request for Quotation
Chemical Name: 2-Cyclopropylpyrimidine-5-carbaldehyde
CAS Number: 954226-60-9
Product Number: AG00IJ21(AGN-PC-04TM33)
Synonyms:
MDL No:
Molecular Formula: C8H8N2O
Molecular Weight: 148.1619

Identification/Properties

Computed Properties
Molecular Weight:
148.165g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
148.064g/mol
Monoisotopic Mass:
148.064g/mol
Topological Polar Surface Area:
42.8A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
148
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
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 2-Cyclopropylpyrimidine-5-carbaldehyde is a versatile chemical compound commonly utilized in chemical synthesis for its unique reactivity and functionality. Due to its distinct cyclopropyl and pyrimidine moieties, this compound serves as a valuable building block in the creation of various molecular structures and pharmaceutical intermediates.In chemical synthesis, 2-Cyclopropylpyrimidine-5-carbaldehyde can be employed as a key precursor in the production of complex organic molecules, such as heterocyclic compounds and medicinal agents. Its cyclopropyl group confers rigidity and steric effects, influencing the selectivity of reactions and the overall three-dimensional shape of the resulting products. Additionally, the pyrimidine ring provides a versatile platform for further functionalization and derivatization, allowing for the synthesis of diverse chemical entities with tailored properties.Overall, the application of 2-Cyclopropylpyrimidine-5-carbaldehyde in chemical synthesis enables chemists to access a wide range of structurally complex molecules and bioactive compounds, making it an essential tool in modern organic chemistry research and drug discovery processes.