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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, 4-(2-propenyloxy)-

C=CCOc1ccc(cc1)C=O Request for Quotation
Chemical Name: Benzaldehyde, 4-(2-propenyloxy)-
CAS Number: 40663-68-1
Product Number: AG003KN8(AGN-PC-0JM1L4)
Synonyms:
MDL No:
Molecular Formula: C10H10O2
Molecular Weight: 162.1852

Identification/Properties

Properties
MP:
150-152℃ (18 TORR)
BP:
150-152 °C18 mm Hg(lit.)
Storage:
Inert atmosphere;Room Temperature;
Form:
Liquid
Stability:
Air Sensitive
Refractive Index:
n20/D 1.568(lit.)
Computed Properties
Molecular Weight:
162.188g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
4
Exact Mass:
162.068g/mol
Monoisotopic Mass:
162.068g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
146
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#:
-
Hazard Statements:
H317
Precautionary Statements:
P280
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(Allyloxy)benzaldehyde is a versatile compound widely used in chemical synthesis for its unique reactivity and functionality. This compound serves as a valuable building block in the creation of various organic compounds due to its ability to participate in a range of key reactions.One of the primary applications of 4-(Allyloxy)benzaldehyde is in the synthesis of heterocycles. By utilizing this compound as a starting material, chemists can efficiently access a variety of heterocyclic structures through cyclization reactions. The allyloxy group present in the molecule can be strategically manipulated to introduce additional functionality or stereochemistry, allowing for the synthesis of diverse heterocyclic scaffolds with tailored properties.Additionally, 4-(Allyloxy)benzaldehyde can be employed in the construction of biologically active molecules and natural product derivatives. Its versatile reactivity enables the modification of the benzaldehyde core to introduce specific moieties or functional groups that are crucial for enhancing the biological activity or pharmacological profile of the target molecule. This versatility makes it a valuable tool for medicinal chemists and researchers in the drug discovery field.Furthermore, this compound plays a vital role in the development of new materials. By leveraging the reactivity of 4-(Allyloxy)benzaldehyde, researchers can access precursors for the synthesis of polymers, dendrimers, and functionalized materials with tailored properties. The allyloxy group can be utilized as a site for polymerization or crosslinking reactions, leading to the formation of novel materials with specific applications in areas such as coatings, adhesives, and sensors.Overall, the application of 4-(Allyloxy)benzaldehyde in chemical synthesis spans a diverse range of fields, and its versatility and reactivity make it a valuable tool for the design and preparation of complex organic molecules, heterocycles, biologically active compounds, and functional materials.