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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, (3,4-dichlorophenyl)-, monohydrochloride

NNc1ccc(c(c1)Cl)Cl.Cl Request for Quotation
Chemical Name: Hydrazine, (3,4-dichlorophenyl)-, monohydrochloride
CAS Number: 19763-90-7
Product Number: AG002AX4(AGN-PC-0QP6GE)
Synonyms:
MDL No:
Molecular Formula: C6H7Cl3N2
Molecular Weight: 213.4922

Identification/Properties

Properties
MP:
230 °C (dec.)(lit.)
BP:
288.3°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
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#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3,4-Dichlorophenylhydrazine Hydrochloride is a versatile compound commonly used in chemical synthesis. It serves as a key building block in the production of various pharmaceutical intermediates and organic compounds. In chemical synthesis, this compound acts as a valuable reagent for the preparation of heterocyclic molecules, specifically pyrazoles and related derivatives. Its ability to undergo diverse reactions, such as nucleophilic substitution and condensation reactions, makes it a valuable tool for the efficient and precise synthesis of complex organic molecules. Additionally, 3,4-Dichlorophenylhydrazine Hydrochloride is widely utilized in the development of agrochemicals, dyes, and other specialty chemicals due to its unique chemical properties and reactivity.