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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-chlorophenyl)-, monohydrochloride

NNc1cccc(c1)Cl.Cl Request for Quotation
Chemical Name: Hydrazine, (3-chlorophenyl)-, monohydrochloride
CAS Number: 2312-23-4
Product Number: AG002M8W(AGN-PC-0QZK9O)
Synonyms:
MDL No:
Molecular Formula: C6H8Cl2N2
Molecular Weight: 179.0471

Identification/Properties

Properties
MP:
240-245 °C (dec.)(lit.)
BP:
266°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
179.044g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
178.006g/mol
Monoisotopic Mass:
178.006g/mol
Topological Polar Surface Area:
38A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
87.1
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


3-Chlorophenylhydrazine Hydrochloride is a versatile compound commonly employed in chemical synthesis for its unique reactivity and functionality. As a key intermediate in organic chemistry, this compound serves as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. Its ability to undergo diverse chemical transformations such as acylation, alkylation, and condensation reactions makes it a crucial reagent in the synthesis of complex molecules. Additionally, 3-Chlorophenylhydrazine Hydrochloride can be utilized in the development of novel materials and as a catalyst in certain organic transformations. Its strategic role in chemical synthesis processes highlights its significance in the pharmaceutical and chemical industries, contributing to the advancement of drug discovery and materials science.