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Brc1cnc(nc1)C
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CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
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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
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Methanone, [2-hydroxy-4-(octyloxy)phenyl]phenyl-

CCCCCCCCOc1ccc(c(c1)O)C(=O)c1ccccc1 Request for Quotation
Chemical Name: Methanone, [2-hydroxy-4-(octyloxy)phenyl]phenyl-
CAS Number: 1843-05-6
Product Number: AG007SBQ(AGN-PC-0JKCIE)
Synonyms:
MDL No:
Molecular Formula: C21H26O3
Molecular Weight: 326.4293

Identification/Properties

Computed Properties
Molecular Weight:
326.436g/mol
XLogP3:
6.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
10
Exact Mass:
326.188g/mol
Monoisotopic Mass:
326.188g/mol
Topological Polar Surface Area:
46.5A^2
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
349
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


The compound (2-Hydroxy-4-(octyloxy)phenyl)(phenyl)methanone, also known as $name$, plays a crucial role in chemical synthesis as a versatile organic reagent. With its unique structure and reactivity, $name$ is commonly used as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and functional materials. Its hydroxy and phenyl groups make it a valuable starting material for the preparation of more complex molecules through functional group transformations such as acylation, alkylation, and reduction reactions. Additionally, the octyloxy side chain provides $name$ with improved solubility and compatibility in different reaction conditions, making it a preferred choice in organic synthesis processes.