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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, (3,5-dichlorophenyl)-, monohydrochloride

NNc1cc(Cl)cc(c1)Cl.Cl Request for Quotation
Chemical Name: Hydrazine, (3,5-dichlorophenyl)-, monohydrochloride
CAS Number: 63352-99-8
Product Number: AG0038KU(AGN-PC-0T81VZ)
Synonyms:
MDL No:
Molecular Formula: C6H7Cl3N2
Molecular Weight: 213.4922

Identification/Properties

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:
99.9
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:
H302-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


3,5-Dichlorophenylhydrazine hydrochloride, also known as $name$, serves as a crucial reagent in chemical synthesis due to its versatile applications. This compound is commonly utilized in organic chemistry as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and reactivity make it a valuable building block for the synthesis of complex molecules, allowing chemists to efficiently access a wide range of novel compounds. Additionally, $name$ is employed in the development of new materials and dyes, showcasing its importance in the field of chemical synthesis. Moreover, its selective reactivity and compatibility with a variety of functional groups make it a valuable tool for organic chemists seeking to streamline synthetic routes and enhance overall efficiency.