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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-amino-2-(3-methoxyphenyl)ethanol;hydrochloride

OCC(c1cccc(c1)OC)N.Cl Request for Quotation
Chemical Name: 2-amino-2-(3-methoxyphenyl)ethanol;hydrochloride
CAS Number: 1187932-17-7
Product Number: AG0092EU(AGN-PC-09RR68)
Synonyms:
MDL No:
Molecular Formula: C9H14ClNO2
Molecular Weight: 203.6660

Identification/Properties

Computed Properties
Molecular Weight:
203.666g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
203.071g/mol
Monoisotopic Mass:
203.071g/mol
Topological Polar Surface Area:
55.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
130
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Amino-2-(3-methoxyphenyl)ethanol hydrochloride, commonly known as $name$, is a versatile compound frequently utilized in chemical synthesis. Its application in organic chemistry primarily revolves around its ability to serve as a key intermediate in the creation of various pharmaceuticals, agrochemicals, and fine chemicals. The compound's unique structure allows for the introduction of functional groups and the formation of complex molecular architectures, making it a valuable building block in the synthesis of biologically active compounds. Furthermore, $name$ can be employed in the preparation of chiral molecules and heterocycles, enhancing its utility in diverse synthetic pathways. Its role in chemical synthesis extends to the development of novel materials and the production of specialized reagents, highlighting its significance in modern organic chemistry practices.