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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-Furanpropanoic acid, a-amino-, hydrochloride (1:1), (aS)-

OC(=O)[C@H](Cc1ccco1)N.Cl Request for Quotation
Chemical Name: 2-Furanpropanoic acid, a-amino-, hydrochloride (1:1), (aS)-
CAS Number: 127682-08-0
Product Number: AG000XA1(AGN-PC-0PILEW)
Synonyms:
MDL No:
Molecular Formula: C7H10ClNO3
Molecular Weight: 191.6122

Identification/Properties

Computed Properties
Molecular Weight:
155.153g/mol
XLogP3:
-2.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
155.058g/mol
Monoisotopic Mass:
155.058g/mol
Topological Polar Surface Area:
76.5A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
149
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-2-Amino-3-(furan-2-yl)propanoic acid hydrochloride is a versatile compound commonly utilized in chemical synthesis processes. Its unique structure, featuring both an amino group and a furan ring, allows for selective reactivity in various reactions. One prominent application of (S)-2-Amino-3-(furan-2-yl)propanoic acid hydrochloride is as a chiral building block in the synthesis of pharmaceuticals and fine chemicals. The chiral nature of this compound enables it to be incorporated into molecules with specific stereochemical preferences, which is crucial for the biological activity and efficacy of the final products.Furthermore, (S)-2-Amino-3-(furan-2-yl)propanoic acid hydrochloride can serve as a key intermediate in the synthesis of complex organic molecules, such as amino acids and peptides. Its ability to undergo various transformations under controlled conditions makes it a valuable tool for chemists seeking to construct intricate molecular architectures with high precision.Overall, the unique structural features and versatile reactivity of (S)-2-Amino-3-(furan-2-yl)propanoic acid hydrochloride make it an indispensable component in the toolkit of synthetic chemists involved in the design and development of novel chemical entities.