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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, 5-fluoro-2-nitro-

OCc1cc(F)ccc1[N+](=O)[O-] Request for Quotation
Chemical Name: Benzenemethanol, 5-fluoro-2-nitro-
CAS Number: 287121-32-8
Product Number: AG002W7J(AGN-PC-00JPSX)
Synonyms:
MDL No: MFCD06202666
Molecular Formula: C7H6FNO3
Molecular Weight: 171.1258

Identification/Properties

Computed Properties
Molecular Weight:
171.127g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
171.033g/mol
Monoisotopic Mass:
171.033g/mol
Topological Polar Surface Area:
66A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
171
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-H320-H335
Precautionary Statements:
P264-P270-P301+P312-P330
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Fluoro-2-nitrobenzyl Alcohol, also known as $name$, serves as a versatile building block in chemical synthesis. Its high reactivity and unique molecular structure make it a valuable reagent in various organic transformations. In the realm of chemical synthesis, 5-Fluoro-2-nitrobenzyl Alcohol is predominantly utilized as a key intermediate in the preparation of pharmaceutical compounds, agrochemicals, and advanced materials. It participates in a range of reactions including nucleophilic substitutions, reductions, and coupling reactions, enabling the construction of complex molecular architectures. By harnessing the chemical properties of 5-Fluoro-2-nitrobenzyl Alcohol, chemists can access diverse chemical space and expedite the synthesis of target molecules with precision and efficiency.