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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-3-(4-methoxyphenyl)propan-1-ol

OCC(Cc1ccc(cc1)OC)N Request for Quotation
Chemical Name: 2-amino-3-(4-methoxyphenyl)propan-1-ol
CAS Number: 176035-15-7
Product Number: AG0021DB(AGN-PC-001CFJ)
Synonyms:
MDL No:
Molecular Formula: C10H15NO2
Molecular Weight: 181.2316

Identification/Properties

Computed Properties
Molecular Weight:
181.235g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
181.11g/mol
Monoisotopic Mass:
181.11g/mol
Topological Polar Surface Area:
55.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
133
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:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Amino-3-(4-methoxyphenyl)propan-1-ol, also known as $name$, serves as a versatile building block in chemical synthesis. With its unique structure, this compound finds wide application in the formation of complex organic molecules. One key use of 2-Amino-3-(4-methoxyphenyl)propan-1-ol is as a valuable intermediate in the synthesis of pharmaceutical compounds, particularly those targeting the central nervous system. Its functional groups enable efficient attachment of various substituents, allowing for the creation of diverse drug candidates. Additionally, this compound can participate in reactions such as acylation, alkylation, and reductive amination, further expanding its synthetic utility in medicinal chemistry and beyond.