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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)-

Benzeneethanol, 4-methyl-

OCCc1ccc(cc1)C Request for Quotation
Chemical Name: Benzeneethanol, 4-methyl-
CAS Number: 699-02-5
Product Number: AG003B2D(AGN-PC-0JM17P)
Synonyms:
MDL No:
Molecular Formula: C9H12O
Molecular Weight: 136.1910

Identification/Properties

Properties
BP:
243.5±8.0°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Refractive Index:
n20/D 1.526(lit.)
Computed Properties
Molecular Weight:
136.194g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
136.089g/mol
Monoisotopic Mass:
136.089g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
82.7
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


2-(p-Tolyl)ethanol, also known as para-tolyl alcohol, is a versatile compound commonly used in various chemical synthesis processes. One of the key applications of this compound is as a building block in the synthesis of pharmaceuticals, agrochemicals, and fragrances. Its unique chemical structure and reactivity make it a valuable intermediate in the production of many important compounds.In organic synthesis, 2-(p-Tolyl)ethanol can undergo various reactions such as oxidation, esterification, and halogenation to yield a wide range of derivatives with different functional groups. These derivatives can then be further modified and used in the development of new molecules with desired properties.Additionally, 2-(p-Tolyl)ethanol can be used as a solvent or reagent in certain chemical transformations due to its ability to solubilize both polar and non-polar compounds. Its mild odor and relatively low toxicity also make it a preferred choice in certain applications where product purity and safety are crucial factors.Overall, 2-(p-Tolyl)ethanol plays a crucial role in the field of chemical synthesis, enabling the creation of diverse compounds with various applications in industry and research.