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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)-

Benzenemethanol, a-methyl-3-(phenylmethoxy)-

CC(c1cccc(c1)OCc1ccccc1)O Request for Quotation
Chemical Name: Benzenemethanol, a-methyl-3-(phenylmethoxy)-
CAS Number: 320727-36-4
Product Number: AG007HEU(AGN-PC-0R7ESC)
Synonyms:
MDL No:
Molecular Formula: C15H16O2
Molecular Weight: 228.2863

Identification/Properties

Computed Properties
Molecular Weight:
228.291g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
4
Exact Mass:
228.115g/mol
Monoisotopic Mass:
228.115g/mol
Topological Polar Surface Area:
29.5A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
211
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(3-(Benzyloxy)phenyl)ethanol is a versatile compound widely used in chemical synthesis due to its unique properties and functional groups. It serves as a valuable building block in the creation of various organic molecules and pharmaceutical intermediates. In organic synthesis, this compound can be utilized as a key reagent in the formation of complex structures, such as heterocycles and chiral compounds. Its benzyl protecting group offers selectivity in reactions and allows for controlled modifications at specific positions in the molecule. Furthermore, the hydroxyl group in 1-(3-(Benzyloxy)phenyl)ethanol makes it a useful precursor for the synthesis of esters, ethers, and other functionalized derivatives. This compound plays a crucial role in the development of novel materials, fine chemicals, and pharmaceutical products.