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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)-

(2S)​-​2-​amino-​2-​(3-​methoxyphenyl)​ethanol

OC[C@H](c1cccc(c1)OC)N.Cl Request for Quotation
Chemical Name: (2S)​-​2-​amino-​2-​(3-​methoxyphenyl)​ethanol
CAS Number: 1213016-49-9
Product Number: AG009Z9S(AGN-PC-0WALYX)
Synonyms:
MDL No:
Molecular Formula: C9H14ClNO2
Molecular Weight: 203.6660

Identification/Properties

Computed Properties
Molecular Weight:
167.208g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
167.095g/mol
Monoisotopic Mass:
167.095g/mol
Topological Polar Surface Area:
55.5A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
130
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
Undefined Atom Stereocenter Count:
0
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#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(2S)-2-amino-2-(3-methoxyphenyl)ethanol is a versatile compound commonly utilized in chemical synthesis as a chiral building block. This compound is invaluable in the creation of pharmaceuticals, agrochemicals, and fine chemicals due to its asymmetric properties. Its unique chiral structure allows for precise control over stereochemistry in organic reactions, making it a key player in the development of advanced materials and bioactive molecules. Additionally, (2S)-2-amino-2-(3-methoxyphenyl)ethanol serves as a crucial intermediate in the synthesis of various amino alcohols, amino acids, and other complex organic compounds. Its role in chemical synthesis highlights its significance in modern chemistry research and applications.