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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-(4-chlorophenoxy)-

O=Cc1ccc(cc1)Oc1ccc(cc1)Cl Request for Quotation
Chemical Name: Benzaldehyde, 4-(4-chlorophenoxy)-
CAS Number: 61343-99-5
Product Number: AG003K2Y(AGN-PC-0L0ZEC)
Synonyms:
MDL No:
Molecular Formula: C13H9ClO2
Molecular Weight: 232.6624

Identification/Properties

Properties
MP:
54-58℃
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
232.663g/mol
XLogP3:
3.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
232.029g/mol
Monoisotopic Mass:
232.029g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
216
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-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-(4-Chlorophenoxy)benzaldehyde is a versatile compound widely used in chemical synthesis as a key intermediate in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. This compound serves as a vital building block in organic synthesis due to its unique chemical reactivity and structural properties. In the field of medicinal chemistry, it is frequently utilized for the synthesis of drug candidates targeting a range of diseases, including cancer, inflammation, and infectious diseases. Additionally, in the realm of materials science, it plays a crucial role in the development of polymers, dyes, and advanced materials with tailored properties. Its ability to undergo a variety of chemical transformations, such as nucleophilic substitution and condensation reactions, makes it a valuable component in the creation of complex molecular frameworks. With its wide range of applications and synthetic versatility, 4-(4-Chlorophenoxy)benzaldehyde continues to be a cornerstone in the realm of chemical synthesis, driving innovation and discovery in various scientific disciplines.