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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, ([1,1'-biphenyl]-4-yloxy)-, hydrazide

NNC(=O)COc1ccc(cc1)c1ccccc1 Request for Quotation
Chemical Name: Acetic acid, ([1,1'-biphenyl]-4-yloxy)-, hydrazide
CAS Number: 84161-08-0
Product Number: AG004ZIG(AGN-PC-0KAX18)
Synonyms:
MDL No:
Molecular Formula: C14H14N2O2
Molecular Weight: 242.2732

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
242.278g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
242.106g/mol
Monoisotopic Mass:
242.106g/mol
Topological Polar Surface Area:
64.4A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
257
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-([1,1'-Biphenyl]-4-yloxy)acetohydrazide is a versatile compound that finds significant application in chemical synthesis. Its unique chemical structure consisting of a biphenyl group linked to an acetohydrazide moiety imparts distinct properties that make it valuable in various synthetic processes.In chemical synthesis, 2-([1,1'-Biphenyl]-4-yloxy)acetohydrazide serves as a key building block for the creation of novel organic molecules. The biphenyl group provides structural diversity and rigidity, influencing the overall properties of the synthesized compounds. Additionally, the acetohydrazide functionality offers reactivity towards various chemical reactions, allowing for further derivatization and modification of the molecule.This compound can be utilized in the preparation of pharmaceutical intermediates, agrochemicals, and materials with tailored properties. Its presence in the synthesis pathway can impact the pharmacological activity, stability, and solubility of the final products. Moreover, the incorporation of 2-([1,1'-Biphenyl]-4-yloxy)acetohydrazide in organic synthesis can lead to the development of compounds with improved biological or physical characteristics.Overall, the application of 2-([1,1'-Biphenyl]-4-yloxy)acetohydrazide in chemical synthesis opens up opportunities for the creation of diverse compounds with potential implications in various industries, making it a valuable tool for synthetic chemists.