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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)-

Pyridine, 2,2'-[1,4-phenylenebis(oxy)]bis[3,5-dichloro-

Clc1cnc(c(c1)Cl)Oc1ccc(cc1)Oc1ncc(cc1Cl)Cl Request for Quotation
Chemical Name: Pyridine, 2,2'-[1,4-phenylenebis(oxy)]bis[3,5-dichloro-
CAS Number: 76150-91-9
Product Number: AG005FF6(AGN-PC-0JK785)
Synonyms:
MDL No: MFCD00057368
Molecular Formula: C16H8Cl4N2O2
Molecular Weight: 402.0589

Identification/Properties

Properties
Form:
Solid
Computed Properties
Molecular Weight:
402.052g/mol
XLogP3:
6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
401.931g/mol
Monoisotopic Mass:
399.934g/mol
Topological Polar Surface Area:
44.2A^2
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
362
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#:
-
Hazard Statements:
H315-H319
Precautionary Statements:
P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313-P362
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1,4-Bis((3,5-dichloropyridin-2-yl)oxy)benzene is a versatile compound commonly used in chemical synthesis as a building block for the creation of various organic molecules. Its unique structure contains two pyridine rings attached to a central benzene ring, each bearing dichloro substituents. This compound is particularly valued in organic synthesis for its ability to act as a cross-coupling reagent in the formation of carbon-carbon bonds. By utilizing 1,4-Bis((3,5-dichloropyridin-2-yl)oxy)benzene, chemists can efficiently construct complex organic frameworks and tailor-made molecules with specific properties for a wide range of applications. Its role in chemical synthesis extends to the development of pharmaceuticals, agrochemicals, advanced materials, and other industrially significant products. The compound's compatibility with a variety of reaction conditions and its versatility make it a valuable tool in the hands of synthetic chemists seeking to explore new pathways and develop innovative chemical solutions.