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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)-

Hydrazine, (2,4-dichlorophenyl)-, monohydrochloride

NNc1ccc(cc1Cl)Cl.Cl Request for Quotation
Chemical Name: Hydrazine, (2,4-dichlorophenyl)-, monohydrochloride
CAS Number: 5446-18-4
Product Number: AG0032Z9(AGN-PC-0SHAL8)
Synonyms:
MDL No:
Molecular Formula: C6H7Cl3N2
Molecular Weight: 213.4922

Identification/Properties

Properties
MP:
220-224 °C(lit.);
BP:
268.8°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
213.486g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
211.967g/mol
Monoisotopic Mass:
211.967g/mol
Topological Polar Surface Area:
38A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
110
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,4-Dichlorophenylhydrazine Hydrochloride is a versatile compound widely used in chemical synthesis for its unique properties. This compound serves as a valuable building block in the creation of various organic molecules and pharmaceuticals. By utilizing the reactivity of the hydrazine functional group, 2,4-Dichlorophenylhydrazine Hydrochloride can be employed in the preparation of hydrazones, which are important intermediates in the synthesis of diverse compounds. Additionally, this compound can participate in the formation of hydrazones with aldehydes and ketones, a key step in the modification of organic molecules. Its ability to facilitate these reactions makes 2,4-Dichlorophenylhydrazine Hydrochloride a crucial component in the toolkit of synthetic chemists, enabling the formation of novel structures and the development of innovative chemical processes.