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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)-

Benzoic acid, 2-hydroxy-, [(2-hydroxyphenyl)methylene]hydrazide

Oc1ccccc1/C=N/NC(=O)c1ccccc1O Request for Quotation
Chemical Name: Benzoic acid, 2-hydroxy-, [(2-hydroxyphenyl)methylene]hydrazide
CAS Number: 3232-36-8
Product Number: AG003U6U(AGN-PC-0O8WQE)
Synonyms:
MDL No:
Molecular Formula: C14H12N2O3
Molecular Weight: 256.2567

Identification/Properties

Computed Properties
Molecular Weight:
256.261g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
256.085g/mol
Monoisotopic Mass:
256.085g/mol
Topological Polar Surface Area:
81.9A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
333
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
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


Salicylidenesalicylhydrazide, also known as SSAH, is a versatile compound widely used in chemical synthesis for its unique properties. One key application of salicylidenesalicylhydrazide is as a ligand in coordination chemistry. Its ability to form stable complexes with metal ions makes it valuable in catalytic processes and coordination polymer synthesis.In organic synthesis, salicylidenesalicylhydrazide is utilized as a chelating agent for various metal ions, such as iron, copper, and nickel. This chelation property enables precise control over the reaction conditions and selectivity, facilitating the synthesis of complex organic compounds.Furthermore, salicylidenesalicylhydrazide has been employed in the preparation of functional materials, such as metal-organic frameworks (MOFs), due to its coordination abilities and structural versatility. These materials have applications in gas storage, separation, and catalysis.Overall, salicylidenesalicylhydrazide plays a crucial role in chemical synthesis by acting as a bridging ligand, enhancing the efficiency and selectivity of various reactions and contributing to the development of new materials with diverse applications.