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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-amino-2,3-difluoro-

Nc1ccc(c(c1O)F)F Request for Quotation
Chemical Name: Phenol, 6-amino-2,3-difluoro-
CAS Number: 115551-33-2
Product Number: AG000G59(AGN-PC-0KKYW2)
Synonyms:
MDL No:
Molecular Formula: C6H5F2NO
Molecular Weight: 145.1068

Identification/Properties

Computed Properties
Molecular Weight:
145.109g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
145.034g/mol
Monoisotopic Mass:
145.034g/mol
Topological Polar Surface Area:
46.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
122
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-H335
Precautionary Statements:
P261-P301+P312-P302+P352-P304+P340-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Amino-2,3-difluorophenol, also known as $name$, is a key compound widely used in chemical synthesis due to its unique properties and versatile applications. This compound plays a crucial role in organic chemistry for the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. Its primary function lies in its ability to serve as a valuable building block in the formation of complex organic molecules.In chemical synthesis, $name$ is utilized as a key intermediate in the preparation of fluorinated organic compounds, which often exhibit enhanced biological activities and increased stability. Its amino and difluorophenol groups provide opportunities for selective functionalization and further derivatization, allowing chemists to tailor the molecule according to specific requirements.Moreover, the presence of amino and difluorophenol moieties in $name$ enables it to participate in a wide range of organic reactions such as nucleophilic substitution, condensation, and coupling reactions. These reactivity profiles make it a versatile starting material for the construction of diverse chemical structures with desired properties.Overall, the application of 6-Amino-2,3-difluorophenol in chemical synthesis offers a valuable platform for the development of novel compounds with potential applications in pharmaceuticals, materials science, and other fields that benefit from the unique properties of fluorinated organic molecules.