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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-Thiophenepropanoic acid, a-amino-b-hydroxy-

OC(=O)C(C(c1cccs1)O)N Request for Quotation
Chemical Name: 2-Thiophenepropanoic acid, a-amino-b-hydroxy-
CAS Number: 32595-59-8
Product Number: AG00BY9K(AGN-PC-0R7VHD)
Synonyms:
MDL No:
Molecular Formula: C7H9NO3S
Molecular Weight: 187.2163

Identification/Properties

Computed Properties
Molecular Weight:
187.213g/mol
XLogP3:
-2.8
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
187.03g/mol
Monoisotopic Mass:
187.03g/mol
Topological Polar Surface Area:
112A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
176
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
2
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Amino-3-hydroxy-3-(thiophen-2-yl)propanoic acid, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. Its unique structure containing an amino group, a hydroxyl group, and a thiophene ring provides it with diverse reactivity and functionality in synthetic pathways.In chemical synthesis, $name$ is commonly used as a key intermediate in the production of pharmaceutical compounds, agrochemicals, and materials with specialized properties. Its amino group can be selectively modified to introduce various functional groups, allowing for the creation of a wide range of organic molecules. Furthermore, the presence of the thiophene ring enhances the aromaticity and electron density of the molecule, leading to enhanced stability and reactivity in certain reactions.$name$ is particularly valued in the pharmaceutical industry for its potential to be incorporated into drug candidates with improved pharmacokinetic profiles and target specificity. By leveraging its unique chemical properties, chemists can design innovative synthetic routes to access complex molecules efficiently and cost-effectively.Overall, the application of 2-Amino-3-hydroxy-3-(thiophen-2-yl)propanoic acid in chemical synthesis highlights its significance as a valuable building block for the creation of advanced materials and biologically active compounds.