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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)-

(S)-2-Amino-3-(2-hydroxyphenyl)propanoic acid hydrochloride

OC(=O)[C@H](Cc1ccccc1O)N.Cl Request for Quotation
Chemical Name: (S)-2-Amino-3-(2-hydroxyphenyl)propanoic acid hydrochloride
CAS Number: 1810074-88-4
Product Number: AG0022LD(AGN-PC-0WAM9D)
Synonyms:
MDL No:
Molecular Formula: C9H12ClNO3
Molecular Weight: 217.6495

Identification/Properties

Computed Properties
Molecular Weight:
217.649g/mol
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
217.051g/mol
Monoisotopic Mass:
217.051g/mol
Topological Polar Surface Area:
83.6A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
184
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-2-Amino-3-(2-hydroxyphenyl)propanoic acid hydrochloride is a versatile compound used extensively in chemical synthesis. This compound plays a crucial role as a chiral building block in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and stereochemistry make it a valuable starting material for the preparation of important molecules in a stereoselective manner.This compound can be utilized in the preparation of chiral ligands, asymmetric catalysts, and pharmacologically active compounds. Its presence in a molecule can impart specific biological activities and enhance the potency of drugs. Additionally, (S)-2-Amino-3-(2-hydroxyphenyl)propanoic acid hydrochloride can be used in the development of new synthetic methodologies and in the modification of existing synthetic routes to improve efficiency and yield.In summary, (S)-2-Amino-3-(2-hydroxyphenyl)propanoic acid hydrochloride is an indispensable tool in chemical synthesis, enabling the creation of complex molecules with desired stereochemical properties and biological activities. Its versatile applications make it a valuable component in the arsenal of chemists and researchers working in the fields of organic synthesis and medicinal chemistry.