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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, 2-chloro-6-fluoro-

OCc1c(F)cccc1Cl Request for Quotation
Chemical Name: Benzenemethanol, 2-chloro-6-fluoro-
CAS Number: 56456-50-9
Product Number: AG003B7D(AGN-PC-0JLZDH)
Synonyms:
MDL No:
Molecular Formula: C7H6ClFO
Molecular Weight: 160.5733

Identification/Properties

Properties
MP:
40-43 °C
BP:
227.6°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
160.572g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
160.009g/mol
Monoisotopic Mass:
160.009g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
110
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:
H315-H319
Precautionary Statements:
P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


With its unique chemical structure and properties, (2-Chloro-6-fluorophenyl)methanol plays a crucial role in various chemical synthesis applications. This compound is widely utilized as a versatile building block in the creation of pharmaceuticals, agrochemicals, and specialty chemicals. Its functional groups make it an essential intermediate for the synthesis of complex organic molecules, enabling the formation of new chemical entities with specific biological or industrial properties. Additionally, (2-Chloro-6-fluorophenyl)methanol can serve as a key reagent in the development of advanced materials and fine chemicals, contributing to the advancement of diverse research fields. Its strategic placement within molecular structures allows for precise modifications and derivatizations, making it a valuable tool for synthetic chemists seeking to design and produce novel compounds with tailored properties and functions.