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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)-

(4-Chloro-naphthalen-1-yl)-hydrazine hydrochloride

NNc1ccc(c2c1cccc2)Cl.Cl Request for Quotation
Chemical Name: (4-Chloro-naphthalen-1-yl)-hydrazine hydrochloride
CAS Number: 1187928-20-6
Product Number: AG01DN9I(AGN-PC-0WALKO)
Synonyms:
MDL No:
Molecular Formula: C10H10Cl2N2
Molecular Weight: 229.1058

Identification/Properties

Computed Properties
Molecular Weight:
229.104g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
228.022g/mol
Monoisotopic Mass:
228.022g/mol
Topological Polar Surface Area:
38A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
174
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound (4-Chloronaphthalen-1-yl)hydrazine hydrochloride is a versatile reagent widely utilized in chemical synthesis for the preparation of various organic compounds. Its applicability spans across multiple areas within the field of chemistry, including medicinal chemistry, agrochemical synthesis, and material science. In chemical synthesis, this compound serves as a valuable building block for creating structurally diverse molecules with potentially beneficial properties. Its unique structure and reactivity enable the formation of complex molecular architectures through versatile synthetic routes, making it an indispensable tool for organic chemists striving to develop novel compounds with desired functionalities.