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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)-

1,3,5-Benzenetriol, 2-nitro-

Oc1cc(O)cc(c1[N+](=O)[O-])O Request for Quotation
Chemical Name: 1,3,5-Benzenetriol, 2-nitro-
CAS Number: 16600-92-3
Product Number: AG003HT4(AGN-PC-0JLVQL)
Synonyms:
MDL No:
Molecular Formula: C6H5NO5
Molecular Weight: 171.1076

Identification/Properties

Properties
MP:
189-193 °C(lit.)
BP:
343°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
171.108g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
0
Exact Mass:
171.017g/mol
Monoisotopic Mass:
171.017g/mol
Topological Polar Surface Area:
107A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
167
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


2-Nitrobenzene-1,3,5-triol, commonly known as phloroglucinol, is a versatile compound that finds extensive application in chemical synthesis. This compound serves as a valuable building block in the production of various pharmaceuticals, fragrances, and organic compounds. In chemical synthesis, 2-Nitrobenzene-1,3,5-triol is frequently employed as a reagent in the creation of complex molecules due to its unique structure and reactivity. Its trihydroxybenzene motif allows it to participate in numerous reactions, including the formation of heterocyclic compounds through cyclization reactions. Additionally, the presence of nitro groups in its structure enables it to act as a precursor for the synthesis of diverse nitrogen-containing compounds. Its ability to undergo multiple functional group transformations makes 2-Nitrobenzene-1,3,5-triol a valuable tool in the hands of synthetic chemists for the preparation of intricate organic molecules with important applications in various industries.