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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)-

Butanoic acid, 3-hydroxy-4-iodo-, ethyl ester, (3S)-

CCOC(=O)C[C@@H](CI)O Request for Quotation
Chemical Name: Butanoic acid, 3-hydroxy-4-iodo-, ethyl ester, (3S)-
CAS Number: 112100-39-7
Product Number: AG008R7V(AGN-PC-0NXTYJ)
Synonyms:
MDL No:
Molecular Formula: C6H11IO3
Molecular Weight: 258.0542

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-Ethyl 3-hydroxy-4-iodobutanoate is a valuable compound in chemical synthesis due to its chiral nature and versatile reactivity. This compound serves as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Its chiral center offers opportunities for creating enantiopure molecules, which are crucial in the development of drugs and other high-value compounds. In addition, the presence of the iodine atom provides a site for further functionalization through various substitution reactions, enabling the creation of complex molecular structures. Overall, (S)-Ethyl 3-hydroxy-4-iodobutanoate plays a vital role in the synthesis of diverse compounds with specific stereochemical and functional group requirements, making it an essential tool for chemists in the pursuit of new chemical entities.