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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)-

Phenol, 6-chloro-2-fluoro-3-methyl-

Clc1ccc(c(c1O)F)C Request for Quotation
Chemical Name: Phenol, 6-chloro-2-fluoro-3-methyl-
CAS Number: 261762-91-8
Product Number: AG002S20(AGN-PC-0KKVM1)
Synonyms:
MDL No:
Molecular Formula: C7H6ClFO
Molecular Weight: 160.5733

Identification/Properties

Properties
MP:
46-49 °C
BP:
188.6°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
160.572g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
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:
120
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:
Danger
UN#:
3261
Hazard Statements:
H302-H314-H411
Precautionary Statements:
P264-P270-P271-P280-P303+P361+P353-P304+P340-P305+P351+P338-P310-P330-P331-P363-P403+P233-P501
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Chloro-2-fluoro-3-methylphenol, commonly known as $name$, serves as a versatile building block in chemical synthesis due to its unique chemical properties. This compound plays a crucial role in the development of pharmaceuticals, agrochemicals, and novel organic compounds. $name$ is widely utilized as a key intermediate in the synthesis of various pharmaceutical drugs. Its strategic positioning in drug development processes allows for the introduction of specific functional groups that are essential for enhancing the biological activity and pharmacokinetic properties of the final drug product. Additionally, the presence of both fluorine and chlorine atoms in $name$ confers increased lipophilicity and chemical stability, making it an attractive candidate for drug design.In the field of agrochemicals, 6-Chloro-2-fluoro-3-methylphenol is instrumental in the creation of crop protection agents and pesticides. Its structural features enable the synthesis of active ingredients that target specific pests or diseases while minimizing environmental impact. By incorporating $name$ into the chemical structure of agrochemicals, researchers can tailor their properties for enhanced efficacy and selectivity.Furthermore, the application of 6-Chloro-2-fluoro-3-methylphenol extends to the realm of organic synthesis, where it serves as a valuable precursor for the construction of complex molecules. Chemists can leverage the reactivity of $name$ to introduce diverse functional groups through various reactions such as halogenation, oxidation, or substitution. This versatility allows for the efficient assembly of intricate organic frameworks with precise control over stereochemistry and regioselectivity.Overall, the strategic utilization of 6-Chloro-2-fluoro-3-methylphenol in chemical synthesis highlights its significance as a versatile and indispensable building block for the development of innovative pharmaceuticals, agrochemicals, and organic compounds.