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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)-

(2-phenoxyphenyl)hydrazine;hydrochloride

NNc1ccccc1Oc1ccccc1.Cl Request for Quotation
Chemical Name: (2-phenoxyphenyl)hydrazine;hydrochloride
CAS Number: 109221-96-7
Product Number: AG008RQH(AGN-PC-010L0W)
Synonyms:
MDL No:
Molecular Formula: C12H13ClN2O
Molecular Weight: 236.6974

Identification/Properties

Computed Properties
Molecular Weight:
236.699g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
236.072g/mol
Monoisotopic Mass:
236.072g/mol
Topological Polar Surface Area:
47.3A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
181
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:
Danger
UN#:
1759
Hazard Statements:
H318
Precautionary Statements:
P280-P305+P351+P338+P310
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


(2-Phenoxyphenyl)hydrazine hydrochloride, a key compound in chemical synthesis, is widely utilized as a versatile building block in various organic reactions. Known for its reactivity and selectivity, this compound serves as a crucial intermediate in the synthesis of pharmaceuticals, agrochemicals, and materials. Its unique structure and functional groups make it an ideal starting material for the production of diverse organic molecules with specific biological activities and properties. With its potential to undergo various transformations, (2-Phenoxyphenyl)hydrazine hydrochloride plays a vital role in the development of new synthetic methodologies and the creation of novel compounds with valuable applications across different industries.