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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)-3-AMINO-2-(HYDROXYMETHYL)PROPANOIC ACID

NC[C@H](C(=O)O)CO Request for Quotation
Chemical Name: (S)-3-AMINO-2-(HYDROXYMETHYL)PROPANOIC ACID
CAS Number: 930784-11-5
Product Number: AG003CLP(AGN-PC-0WAJZ3)
Synonyms:
MDL No:
Molecular Formula: C4H9NO3
Molecular Weight: 119.1192

Identification/Properties

Properties
BP:
357.8±32.0°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;

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


(S)-3-Amino-2-(hydroxymethyl)propanoic acid, also known as serine, is a versatile amino acid that plays a crucial role in chemical synthesis. This compound is commonly utilized as a building block in the creation of various biologically active molecules, pharmaceuticals, and natural products. Its unique structural features make it an essential component in peptide synthesis, where it can serve as a key intermediate in the formation of peptide bonds.In the field of medicinal chemistry, (S)-3-Amino-2-(hydroxymethyl)propanoic acid is frequently employed for the synthesis of drugs targeting specific biological pathways. Its amino and hydroxyl functional groups enable the introduction of diverse chemical moieties, allowing for the modification of pharmacological properties such as solubility, bioavailability, and specificity. Additionally, serine's stereochemistry can influence the overall three-dimensional shape of the resulting molecules, impacting their interactions with biological targets.Furthermore, (S)-3-Amino-2-(hydroxymethyl)propanoic acid has been utilized in the development of enzyme inhibitors, receptor ligands, and other therapeutic agents. Its presence in the structures of many naturally occurring proteins and enzymes highlights its importance in mimicking biologically relevant molecules during drug design. The strategic incorporation of serine derivatives in chemical synthesis can lead to the discovery of novel compounds with promising pharmacological activities.Overall, the application of (S)-3-Amino-2-(hydroxymethyl)propanoic acid in chemical synthesis extends beyond its role as a simple amino acid, showcasing its significance in the realm of drug discovery and development.