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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)-

Benzenepropanol, 2-hydroxy-5-methyl-g-phenyl-

OCCC(c1cc(C)ccc1O)c1ccccc1 Request for Quotation
Chemical Name: Benzenepropanol, 2-hydroxy-5-methyl-g-phenyl-
CAS Number: 851789-43-0
Product Number: AG004MWS(AGN-PC-0UYIT7)
Synonyms:
MDL No:
Molecular Formula: C16H18O2
Molecular Weight: 242.3129

Identification/Properties

Properties
MP:
118-120°C
BP:
414.8°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
242.318g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
4
Exact Mass:
242.131g/mol
Monoisotopic Mass:
242.131g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
235
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(3-Hydroxy-1-phenylpropyl)-4-methylphenol, also known as $name$, is a versatile compound widely used in chemical synthesis for its unique properties and applications. In organic chemistry, this compound serves as a key building block for the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. Its hydroxy and phenyl groups make it a valuable intermediate in the production of complex organic molecules through functional group transformations and derivatization reactions. Additionally, the presence of the methyl group provides opportunities for selective modifications and structural diversity in the target molecules. Overall, $name$ plays a crucial role in designing and creating novel compounds with enhanced properties and functions for a wide range of applications in the chemical industry.