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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)-1-Acetyl-3-hydroxypyrrolidine

O[C@H]1CCN(C1)C(=O)C Request for Quotation
Chemical Name: (S)-1-Acetyl-3-hydroxypyrrolidine
CAS Number: 943587-40-4
Product Number: AG003CJO(AGN-PC-0WA2TF)
Synonyms:
MDL No: MFCD09909314
Molecular Formula: C6H11NO2
Molecular Weight: 129.1570

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
129.159g/mol
XLogP3:
-0.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
129.079g/mol
Monoisotopic Mass:
129.079g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
124
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P233-P260-P261-P264-P270-P271-P280-P301+P312-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P330-P332+P313-P337+P313-P340-P362-P403-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-1-(3-Hydroxypyrrolidin-1-yl)ethanone, also known as $name$, is a versatile compound widely utilized in chemical synthesis due to its unique properties. As an enantiomerically pure form of 1-(3-Hydroxypyrrolidin-1-yl)ethanone, this compound plays a crucial role in asymmetric synthesis, where the stereochemistry of the molecule significantly impacts the outcome of reactions.In chemical synthesis, (S)-1-(3-Hydroxypyrrolidin-1-yl)ethanone serves as a chiral building block for the construction of complex organic molecules. Its chiral nature allows for the creation of new compounds with defined stereochemistry, making it an essential component in the production of pharmaceuticals, agrochemicals, and other fine chemicals. By incorporating this compound into synthetic pathways, chemists can control the chirality of the final product, enabling the development of enantiomerically pure substances with specific biological activities.Moreover, the presence of the hydroxyl group in (S)-1-(3-Hydroxypyrrolidin-1-yl)ethanone offers additional reactivity in chemical transformations. The hydroxyl functionality can participate in various reactions such as nucleophilic substitutions, hydrogen bonding, and oxidation reactions, expanding the synthetic possibilities of this compound. Overall, (S)-1-(3-Hydroxypyrrolidin-1-yl)ethanone is a valuable tool in chemical synthesis, allowing chemists to access a diverse range of structurally intricate molecules with high levels of stereochemical control.