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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)-

2,1-Benzoxaborole, 5-fluoro-1,3-dihydro-1-hydroxy-

Fc1ccc2c(c1)COB2O Request for Quotation
Chemical Name: 2,1-Benzoxaborole, 5-fluoro-1,3-dihydro-1-hydroxy-
CAS Number: 174671-46-6
Product Number: AG001ZVO(AGN-PC-00AC3V)
Synonyms:
MDL No:
Molecular Formula: C7H6BFO2
Molecular Weight: 151.9307

Identification/Properties

Computed Properties
Molecular Weight:
151.931g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
152.044g/mol
Monoisotopic Mass:
152.044g/mol
Topological Polar Surface Area:
29.5A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
155
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-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Fluoro-1,3-dihydro-1-hydroxy-2,1-benzoxaborole is a versatile chemical compound widely used in chemical synthesis processes. It serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and materials. Due to its unique structure and reactivity, this compound plays a crucial role in the development of new chemical entities with potential applications in drug discovery and other industries.One of the primary applications of 5-Fluoro-1,3-dihydro-1-hydroxy-2,1-benzoxaborole in chemical synthesis is its ability to participate in organic reactions such as coupling, cyclization, and functional group transformations. Its boron-containing ring structure imparts desirable properties that make it a valuable component in the synthesis of complex molecules. By utilizing the reactivity of the boron atom, chemists can generate novel molecular architectures and functionalized compounds with tailored properties.Furthermore, the presence of the fluorine atom in 5-Fluoro-1,3-dihydro-1-hydroxy-2,1-benzoxaborole enhances its chemical stability and imparts unique electronic characteristics that influence its behavior in chemical reactions. This fluorinated benzoxaborole compound can be employed as a strategic building block in the construction of biologically active molecules, offering opportunities for the development of new drugs and advanced materials.In summary, the versatile nature of 5-Fluoro-1,3-dihydro-1-hydroxy-2,1-benzoxaborole makes it a valuable tool in the field of chemical synthesis, enabling the creation of diverse compounds with potential applications in various industries.