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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-Dioxolane, 2-(4-nitrophenyl)-

[O-][N+](=O)c1ccc(cc1)C1OCCO1 Request for Quotation
Chemical Name: 1,3-Dioxolane, 2-(4-nitrophenyl)-
CAS Number: 2403-53-4
Product Number: AG00BIB5(AGN-PC-0JO03M)
Synonyms:
MDL No:
Molecular Formula: C9H9NO4
Molecular Weight: 195.1721

Identification/Properties

Properties
BP:
332.9°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
195.174g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
195.053g/mol
Monoisotopic Mass:
195.053g/mol
Topological Polar Surface Area:
64.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
201
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-H319
Precautionary Statements:
P261-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(4-Nitrophenyl)-1,3-dioxolane, also known as NPD, is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. This compound serves as a valuable building block in the creation of various organic molecules and materials due to its ability to participate in a range of chemical reactions.One of the key applications of 2-(4-Nitrophenyl)-1,3-dioxolane in chemical synthesis is as a precursor for the synthesis of heterocyclic compounds. By incorporating NPD into the molecular structure, chemists can introduce specific functionalities and increase the complexity of the final product. This versatile compound enables the formation of diverse ring systems, making it a valuable tool in the design and preparation of novel organic compounds.Additionally, 2-(4-Nitrophenyl)-1,3-dioxolane can be utilized as a protecting group in organic synthesis. By temporarily masking reactive functional groups with NPD, chemists can selectively control the reactivity of certain sites in a molecule, allowing for precise modifications and manipulations during chemical reactions. This protective functionality enhances the synthetic efficiency and selectivity of complex organic transformations.Furthermore, the unique reactivity of 2-(4-Nitrophenyl)-1,3-dioxolane lends itself to applications in medicinal chemistry, materials science, and drug development. Its versatile nature and compatibility with various reaction conditions make it a valuable asset in the synthesis of biologically active compounds, functional materials, and pharmaceutical intermediates.In conclusion, 2-(4-Nitrophenyl)-1,3-dioxolane plays a critical role in chemical synthesis by serving as a versatile building block, a protective group, and a key component in the creation of diverse organic molecules. Its applications extend across different fields of chemistry, making it an indispensable tool for researchers and synthetic chemists seeking to explore new frontiers in molecular design and development.