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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, 4-methyl-a-phenyl-

Cc1ccc(cc1)C(c1ccccc1)O Request for Quotation
Chemical Name: Benzenemethanol, 4-methyl-a-phenyl-
CAS Number: 1517-63-1
Product Number: AG003LRB(AGN-PC-0Q662O)
Synonyms:
MDL No:
Molecular Formula: C14H14O
Molecular Weight: 198.2604

Identification/Properties

Properties
MP:
50-54 °C(lit.)
BP:
334.9°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Refractive Index:
1.5381 (estimate)
Computed Properties
Molecular Weight:
198.265g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
198.104g/mol
Monoisotopic Mass:
198.104g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
176
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:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P301+P312-P302+P352-P304+P340-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Phenyl(p-tolyl)methanol is a versatile organic compound commonly used in chemical synthesis for its unique properties and reactivity. In the field of organic chemistry, this compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and advanced materials.Its applications in chemical synthesis are diverse and wide-ranging. One key use of Phenyl(p-tolyl)methanol is as a precursor in the synthesis of chiral ligands, which play a crucial role in asymmetric catalysis. By incorporating this compound into the structure of ligands, chemists can control the stereochemistry of reactions and enhance the selectivity of their processes.Additionally, Phenyl(p-tolyl)methanol is an important intermediate in the production of fine chemicals such as fragrances, flavors, and dyes. Its aromatic structure and functional groups make it a valuable starting material for the synthesis of various complex molecules with specific properties and biological activities.Moreover, this compound can be employed in the preparation of polymers and plastics, where its structure contributes to the desired properties of the final material. By modifying the chemical structure of Phenyl(p-tolyl)methanol, chemists can tailor the properties of polymers to meet specific industrial or commercial requirements.Overall, the utilization of Phenyl(p-tolyl)methanol in chemical synthesis highlights its significance as a key building block in the creation of diverse compounds with valuable applications across different industries, ranging from pharmaceuticals to materials science.