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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)-

Phenanthro[3,4-d]-1,3-dioxole-5-carboxylic acid, 6-nitro-

[O-][N+](=O)c1cc2ccccc2c2c1c(cc1c2OCO1)C(=O)O Request for Quotation
Chemical Name: Phenanthro[3,4-d]-1,3-dioxole-5-carboxylic acid, 6-nitro-
CAS Number: 475-80-9
Product Number: AG00D8TY(AGN-PC-0JLG5D)
Synonyms:
MDL No:
Molecular Formula: C16H9NO6
Molecular Weight: 311.2458

Identification/Properties

Properties
Storage:
2-8℃;
Computed Properties
Molecular Weight:
311.249g/mol
XLogP3:
3.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
1
Exact Mass:
311.043g/mol
Monoisotopic Mass:
311.043g/mol
Topological Polar Surface Area:
102A^2
Heavy Atom Count:
23
Formal Charge:
0
Complexity:
505
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Nitrophenanthro[3,4-d]-1,3-dioxole-5-carboxylic acid is a versatile compound that finds significant application in chemical synthesis. This compound is utilized as a key building block in the development of various pharmaceuticals, agrochemicals, and advanced materials. In chemical synthesis, 6-Nitrophenanthro[3,4-d]-1,3-dioxole-5-carboxylic acid serves as a crucial intermediate in the creation of complex organic molecules due to its unique structural properties and reactivity. Its presence in the synthesis pathway enables the introduction of functional groups, modification of aromatic compounds, and formation of diverse chemical bonds, thereby facilitating the production of valuable compounds with enhanced properties and functionalities. The incorporation of this compound in chemical reactions allows for the efficient and targeted synthesis of specific substances, making it a valuable tool in the hands of synthetic chemists and researchers.