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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, 2,3-difluoro-

OCCc1cccc(c1F)F Request for Quotation
Chemical Name: Benzeneethanol, 2,3-difluoro-
CAS Number: 126163-30-2
Product Number: AG000RWD(AGN-PC-0KKVZT)
Synonyms:
MDL No:
Molecular Formula: C8H8F2O
Molecular Weight: 158.1453

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Computed Properties
Molecular Weight:
158.148g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
158.054g/mol
Monoisotopic Mass:
158.054g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
119
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-(2,3-Difluorophenyl)ethanol is a valuable compound used in chemical synthesis for various applications. One key application of this compound is as a versatile building block in the synthesis of pharmaceuticals and agrochemicals. Its structure contains a difluorophenyl group attached to an ethanol moiety, making it a valuable intermediate in the preparation of a wide range of organic compounds.Due to the presence of the difluorophenyl group, 2-(2,3-Difluorophenyl)ethanol can participate in various organic reactions such as nucleophilic substitution, Grignard reactions, and metal-catalyzed cross-coupling reactions. This compound is particularly useful in the synthesis of molecules with biological activity, where the presence of fluorine atoms can enhance the compound's properties such as lipophilicity, metabolic stability, and binding affinity to biological targets.Furthermore, the hydroxyl group in 2-(2,3-Difluorophenyl)ethanol provides a handle for further functionalization, enabling the incorporation of additional functional groups or modifications to tailor the compound's properties for specific applications. Overall, the versatility and reactivity of 2-(2,3-Difluorophenyl)ethanol make it an essential building block in organic synthesis for the development of new drugs, pesticides, and other bioactive molecules.