1. Home
  2. 1,1':4',1''-Terphenyl, 4-nitro-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

1,1':4',1''-Terphenyl, 4-nitro-

[O-][N+](=O)c1ccc(cc1)c1ccc(cc1)c1ccccc1 Request for Quotation
Chemical Name: 1,1':4',1''-Terphenyl, 4-nitro-
CAS Number: 10355-53-0
Product Number: AG003LWL(AGN-PC-0JKI2L)
Synonyms:
MDL No:
Molecular Formula: C18H13NO2
Molecular Weight: 275.3013

Identification/Properties

Properties
MP:
205-210℃
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
275.307g/mol
XLogP3:
5.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
275.095g/mol
Monoisotopic Mass:
275.095g/mol
Topological Polar Surface Area:
45.8A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
330
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

Request for Quotation

Customer Feedback

Chemical Structure


4-Nitro-1,1':4',1''-terphenyl, also known as $name$, is a versatile compound used in chemical synthesis for its unique properties and reactivity. This compound serves as a crucial building block in the creation of various organic molecules and materials. In the field of organic chemistry, $name$ is commonly employed in the synthesis of complex aromatic compounds, pharmaceutical intermediates, and functional materials.One of the key applications of 4-Nitro-1,1':4',1''-terphenyl in chemical synthesis is as a precursor for the preparation of substituted terphenyl derivatives. By utilizing this compound as a starting material, chemists can introduce different functional groups or modifications at specific positions on the terphenyl backbone. This strategic functionalization enables the synthesis of tailored molecules with desired properties, such as enhanced solubility, improved stability, or specific biological activities.Additionally, 4-Nitro-1,1':4',1''-terphenyl can participate in various cross-coupling reactions, such as Suzuki coupling or Heck reaction, to form aryl-aryl or aryl-vinyl bonds. These transformations are essential for the construction of complex organic frameworks and the assembly of diverse molecular architectures. The versatility of $name$ in these synthetic methodologies makes it a valuable tool for organic chemists pursuing the development of new chemical entities or advanced materials.Overall, the application of 4-Nitro-1,1':4',1''-terphenyl in chemical synthesis offers a wide range of possibilities for creating novel compounds with tailored properties and functionalities. Its role as a key intermediate in organic transformations underscores its importance in advancing the field of synthetic chemistry and innovation in material science.