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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)-

Benzenesulfonic acid, 4-methyl-, (diphenylmethylene)hydrazide

Cc1ccc(cc1)S(=O)(=O)NN=C(c1ccccc1)c1ccccc1 Request for Quotation
Chemical Name: Benzenesulfonic acid, 4-methyl-, (diphenylmethylene)hydrazide
CAS Number: 4545-20-4
Product Number: AG00DIR8(AGN-PC-0JO4WH)
Synonyms:
MDL No:
Molecular Formula: C20H18N2O2S
Molecular Weight: 350.4341

Identification/Properties

Computed Properties
Molecular Weight:
350.436g/mol
XLogP3:
4.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
5
Exact Mass:
350.109g/mol
Monoisotopic Mass:
350.109g/mol
Topological Polar Surface Area:
66.9A^2
Heavy Atom Count:
25
Formal Charge:
0
Complexity:
513
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


Benzophenone tosylhydrazone is a versatile compound that finds common use in chemical synthesis as a reagent for the generation of reactive intermediates. In particular, its ability to form diazo compounds makes it a valuable tool in various organic transformations. When exposed to specific conditions, Benzophenone tosylhydrazone can undergo diazo transfer, leading to the generation of highly reactive carbenes. These carbenes can then participate in a range of reactions including cyclopropanation, ylide formation, and C-H insertion. Additionally, Benzophenone tosylhydrazone has been utilized in the synthesis of various biologically active molecules and natural products, showcasing its significance in designing new compounds with potential pharmaceutical applications.