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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-(octyloxy)-

CCCCCCCCOc1ccc(cc1)C=O Request for Quotation
Chemical Name: Benzaldehyde, 4-(octyloxy)-
CAS Number: 24083-13-4
Product Number: AG003K9W(AGN-PC-0JLYLM)
Synonyms:
MDL No:
Molecular Formula: C15H22O2
Molecular Weight: 234.3340

Identification/Properties

Properties
BP:
349.9°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Stability:
Air Sensitive
Refractive Index:
1.52-1.522
Computed Properties
Molecular Weight:
234.339g/mol
XLogP3:
4.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
9
Exact Mass:
234.162g/mol
Monoisotopic Mass:
234.162g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
183
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:
H317-H319
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(Octyloxy)benzaldehyde, also known as 4-octyloxybenzaldehyde, is a versatile organic compound commonly used in chemical synthesis for various applications. This aldehyde compound features an octyl group attached to the benzene ring, providing unique properties that make it valuable in organic chemistry reactions.In chemical synthesis, 4-(Octyloxy)benzaldehyde serves as a key building block in the production of various functional molecules and materials. Its aldehyde functional group allows for the formation of new carbon-carbon bonds through aldol condensation reactions, making it an essential reagent in the construction of complex organic structures. Additionally, the octyl moiety offers hydrophobic characteristics, which can be advantageous in applications requiring nonpolar properties.Furthermore, 4-(Octyloxy)benzaldehyde can be used as a precursor in the synthesis of aromatic compounds, polymers, and pharmaceutical intermediates. Its versatile nature and reactivity make it a valuable tool for organic chemists looking to design and create novel compounds with specific properties and functionalities.Overall, the application of 4-(Octyloxy)benzaldehyde in chemical synthesis highlights its significance in building molecular complexity and advancing research and development efforts across various industries.