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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-propyl-

CCCc1ccc(cc1)C=O Request for Quotation
Chemical Name: Benzaldehyde, 4-propyl-
CAS Number: 28785-06-0
Product Number: AG002WGM(AGN-PC-0JLMO7)
Synonyms:
MDL No:
Molecular Formula: C10H12O
Molecular Weight: 148.2017

Identification/Properties

Properties
BP:
239.9°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Liquid
Refractive Index:
n20/D 1.532(lit.)
Computed Properties
Molecular Weight:
148.205g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
3
Exact Mass:
148.089g/mol
Monoisotopic Mass:
148.089g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
112
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


4-Propylbenzaldehyde, also known as 4-pentylbenzaldehyde, is a versatile chemical compound widely utilized in chemical synthesis processes. In organic chemistry, 4-Propylbenzaldehyde serves as a key building block for the preparation of various aromatic compounds and derivatives. Its aldehyde functional group enables it to participate in a variety of reactions, making it a valuable intermediate in the synthesis of pharmaceuticals, fragrances, and agrochemicals.One common application of 4-Propylbenzaldehyde is its use in the production of fragrances and flavoring agents. By undergoing reactions such as Friedel-Crafts acylation or nucleophilic addition, this compound can be transformed into more complex aromatic molecules with unique scents and tastes. In the pharmaceutical industry, 4-Propylbenzaldehyde can be employed as a starting material for the synthesis of drug candidates or active pharmaceutical ingredients, contributing to the development of novel therapeutic agents.Additionally, 4-Propylbenzaldehyde plays a crucial role in organic synthesis by serving as a precursor for the preparation of various functionalized aromatic compounds. Through selective modifications and functional group transformations, chemists can harness the reactivity of 4-Propylbenzaldehyde to access a diverse array of products with tailored properties and applications.Overall, the significance of 4-Propylbenzaldehyde in chemical synthesis lies in its versatility and reactivity, allowing for the creation of valuable compounds across different industries and research fields.