(S)-2-Amino-3-(4-vinylphenyl)propanoic acid hydrochloride|1810074-65-7,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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-(4-vinylphenyl)propanoic acid hydrochloride

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Chemical Name:	(S)-2-Amino-3-(4-vinylphenyl)propanoic acid hydrochloride
CAS Number:	1810074-65-7
Product Number:	AG0022KN(AGN-PC-0WAMAB)
Synonyms:
MDL No:
Molecular Formula:	C11H14ClNO2
Molecular Weight:	227.6874

Identification/Properties
Safety Information
NMR Spectrum
Other Analytical Data
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Identification/Properties

Computed Properties

Molecular Weight:

227.69g/mol

Hydrogen Bond Donor Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

Exact Mass:

227.071306g/mol

Monoisotopic Mass:

227.071306g/mol

Topological Polar Surface Area:

63.3Å²

Heavy Atom Count:

Formal Charge:

Complexity:

207

Isotope Atom Count:

Defined Atom Stereocenter Count:

Undefined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Undefined Bond Stereocenter Count:

Covalently-Bonded Unit Count:

Compound Is Canonicalized:

Yes

Safety Information

GHS Pictogram:

Signal Word:

Warning

UN#:

Hazard Statements:

H302-H315-H319-H335

Precautionary Statements:

P261-P305+P351+P338

Class:

Packing Group:

NMR Spectrum

Other Analytical Data

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Chemical Structure

The (S)-2-Amino-3-(4-vinylphenyl)propanoic acid hydrochloride has a crucial role in chemical synthesis as a chiral building block. It serves as a key intermediate in the production of various pharmaceutical compounds, agrochemicals, and specialty chemicals. The chiral nature of this compound makes it particularly valuable in asymmetric synthesis, where the stereochemistry of the molecule significantly impacts the properties and functions of the final product. Additionally, (S)-2-Amino-3-(4-vinylphenyl)propanoic acid hydrochloride can be used in the synthesis of peptides and peptide mimetics, as well as in the preparation of novel materials with tailored properties for specific applications in materials science and drug discovery. By incorporating this compound into synthetic pathways, chemists can access a diverse array of structurally complex and biologically active molecules with high efficiency and selectivity.