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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, 3,5-difluoro-a-methyl-

CC(c1cc(F)cc(c1)F)O Request for Quotation
Chemical Name: Benzenemethanol, 3,5-difluoro-a-methyl-
CAS Number: 872181-59-4
Product Number: AG003CW5(AGN-PC-0VBI4Z)
Synonyms:
MDL No:
Molecular Formula: C8H8F2O
Molecular Weight: 158.1453

Identification/Properties

Properties
Form:
Liquid
Computed Properties
Molecular Weight:
158.148g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
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:
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-H320-H335
Precautionary Statements:
P264-P270-P301+P312-P330
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(3,5-Difluorophenyl)ethanol is a versatile compound that finds wide application in chemical synthesis. With its unique structure and properties, this compound is a valuable building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals. In organic synthesis, it serves as a key intermediate in the production of complex molecules due to its reactivity and ability to undergo diverse chemical transformations. Additionally, 1-(3,5-Difluorophenyl)ethanol can be utilized in the synthesis of novel materials and functionalized organic compounds, making it an essential component in the toolkit of synthetic chemists. Its broad range of applications highlights the significance of this compound in advancing the field of chemical synthesis.