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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)-

1-Naphthaleneacethydrazide

NNC(=O)Cc1cccc2c1cccc2 Request for Quotation
Chemical Name: 1-Naphthaleneacethydrazide
CAS Number: 34800-90-3
Product Number: AG00I6VQ(AGN-PC-0WA4QF)
Synonyms:
MDL No:
Molecular Formula: C12H12N2O
Molecular Weight: 200.2365

Identification/Properties

Properties
MP:
168-169 °C
BP:
466.4°C at 760 mmHg
Storage:
Inert atmosphere;-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
200.241g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
200.095g/mol
Monoisotopic Mass:
200.095g/mol
Topological Polar Surface Area:
55.1A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
230
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-(Naphthalen-1-yl)acetohydrazide, a versatile compound widely used in chemical synthesis, serves as a key building block in various organic reactions. This compound's unique structure enables it to participate in diverse transformations, making it valuable in the synthesis of complex organic molecules. When utilized in chemical reactions, 2-(Naphthalen-1-yl)acetohydrazide demonstrates excellent reactivity and selectivity, allowing for the efficient formation of new carbon-carbon or carbon-nitrogen bonds. Its presence often imparts specific functionalities or structural motifs to the final products, enhancing their properties and potential applications in medicinal chemistry, materials science, and other research fields. In the realm of chemical synthesis, 2-(Naphthalen-1-yl)acetohydrazide stands as a powerful tool for creating novel compounds with tailored structures and functionalities, paving the way for exciting advancements in organic chemistry.