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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)-

Acetic acid, (2-nitrophenoxy)-

OC(=O)COc1ccccc1[N+](=O)[O-] Request for Quotation
Chemical Name: Acetic acid, (2-nitrophenoxy)-
CAS Number: 1878-87-1
Product Number: AG002GHO(AGN-PC-0JKCK4)
Synonyms:
MDL No:
Molecular Formula: C8H7NO5
Molecular Weight: 197.1449

Identification/Properties

Properties
MP:
157-160 °C(lit.)
BP:
388.3°C at 760 mmHg
Storage:
Room Temperature;
Form:
Solid
Refractive Index:
1.5700 (estimate)
Computed Properties
Molecular Weight:
197.146g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
197.032g/mol
Monoisotopic Mass:
197.032g/mol
Topological Polar Surface Area:
92.4A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
224
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
Precautionary Statements:
P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(2-Nitrophenoxy)acetic acid is a versatile compound frequently used in chemical synthesis as a key intermediate in the production of various organic compounds. Its unique structure allows it to participate in a wide range of reactions, making it a valuable building block for the creation of new molecules.One of the primary applications of 2-(2-Nitrophenoxy)acetic acid in chemical synthesis is in the formation of heterocyclic compounds. By reacting this compound with other appropriate reagents, chemists can create a diverse array of heterocycles, which are vital in pharmaceuticals, agrochemicals, and materials science. Additionally, this compound can be utilized in the synthesis of specialty polymers and advanced materials due to its ability to introduce specific functionalities into the final products.Furthermore, 2-(2-Nitrophenoxy)acetic acid is frequently employed in the preparation of various fine chemicals, such as dyes, fragrances, and flavor compounds. Its structural characteristics make it a valuable precursor for introducing aromatic and nitro functionalities into these complex molecules, enhancing their properties and applications.Overall, the application of 2-(2-Nitrophenoxy)acetic acid in chemical synthesis plays a crucial role in the development of novel compounds with diverse functionalities and applications across multiple industries.