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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, 2,6-dichloro-

OCCc1c(Cl)cccc1Cl Request for Quotation
Chemical Name: Benzeneethanol, 2,6-dichloro-
CAS Number: 30595-79-0
Product Number: AG0030MS(AGN-PC-0KK6CY)
Synonyms:
MDL No: MFCD00800674
Molecular Formula: C8H8Cl2O
Molecular Weight: 191.0545

Identification/Properties

Properties
MP:
59-65 °C
BP:
276.6°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Refractive Index:
1.5670 (estimate)
Computed Properties
Molecular Weight:
191.051g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
189.995g/mol
Monoisotopic Mass:
189.995g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
109
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,6-Dichlorophenethyl alcohol is a versatile compound used in various chemical synthesis reactions. In organic chemistry, this compound serves as a valuable building block for the creation of aromatic compounds with diverse functionalities. Its unique structure containing both chlorine groups and a hydroxyl group allows for the introduction of specific chemical properties into target molecules. This compound can be utilized as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. The presence of the chlorinated phenyl group provides opportunities for further derivatization through substitution reactions, allowing chemists to tailor the properties of the final products for specific applications. Additionally, the hydroxyl group can participate in various reactions, such as esterification or etherification, expanding the range of compounds that can be synthesized using 2,6-Dichlorophenethyl alcohol.Overall, the strategic incorporation of 2,6-Dichlorophenethyl alcohol in chemical synthesis enables the synthesis of structurally diverse molecules with enhanced functionalities, making it a valuable tool for organic chemists in the development of novel compounds for a wide range of applications.