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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)-

Ethanone, 1-(3-hydroxyphenyl)-2-(methylamino)-, hydrochloride

CNCC(=O)c1cccc(c1)O.Cl Request for Quotation
Chemical Name: Ethanone, 1-(3-hydroxyphenyl)-2-(methylamino)-, hydrochloride
CAS Number: 94240-17-2
Product Number: AG00GRAL(AGN-PC-0KO0L9)
Synonyms:
MDL No:
Molecular Formula: C9H12ClNO2
Molecular Weight: 201.65008

Identification/Properties

Computed Properties
Molecular Weight:
201.65g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
201.056g/mol
Monoisotopic Mass:
201.056g/mol
Topological Polar Surface Area:
49.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
159
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


1-(3-Hydroxyphenyl)-2-(methylamino)ethanone hydrochloride, also known as $name$, is a versatile chemical compound widely used in chemical synthesis processes. Due to its unique structure and properties, this compound serves as a key intermediate in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. 
Its ability to undergo selective transformations makes it an essential building block in the synthesis of complex organic molecules with diverse applications in the pharmaceutical industry. $name$ enables the introduction of both the hydroxyl and amino groups into target molecules, allowing for the creation of new chemical entities with enhanced biological activities. 
Furthermore, its hydrochloride salt form provides stability and ease of handling during synthesis, making it a preferred choice for chemists and researchers. By incorporating $name$ into synthetic routes, chemists can access a wide range of novel compounds that have the potential to impact various fields of chemistry and biology.