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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-ethylphenyl)-, hydrochloride

NNc1ccccc1CC.Cl Request for Quotation
Chemical Name: Hydrazine, (2-ethylphenyl)-, hydrochloride
CAS Number: 58711-02-7
Product Number: AG00IKEA(AGN-PC-0KK5XK)
Synonyms:
MDL No:
Molecular Formula: C8H13ClN2
Molecular Weight: 172.65522

Identification/Properties

Properties
MP:
178 °C (dec.)(lit.)
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
172.656g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
172.077g/mol
Monoisotopic Mass:
172.077g/mol
Topological Polar Surface Area:
38A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
93.3
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


The (2-Ethylphenyl)hydrazine hydrochloride is a versatile chemical compound used in various chemical synthesis applications. This compound serves as a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals due to its unique reactivity and functional group compatibility. In chemical synthesis, (2-Ethylphenyl)hydrazine hydrochloride can be used as a key intermediate in the preparation of heterocyclic compounds, which are commonly found in pharmaceuticals and bioactive molecules. Additionally, this compound can participate in various organic reactions such as nucleophilic substitution, condensation, and cyclization reactions to form complex molecular structures. Its ability to undergo selective transformations makes it a valuable tool for chemists seeking to design and create novel compounds with specific properties and functionalities.