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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)-

Ethanone, 1-[(3R)-3-hydroxy-1-pyrrolidinyl]-

O[C@@H]1CCN(C1)C(=O)C Request for Quotation
Chemical Name: Ethanone, 1-[(3R)-3-hydroxy-1-pyrrolidinyl]-
CAS Number: 916733-17-0
Product Number: AG003C7U(AGN-PC-0OMUSU)
Synonyms:
MDL No: MFCD09909313
Molecular Formula: C6H11NO2
Molecular Weight: 129.1570

Identification/Properties

Properties
MP:
83 °C
BP:
286.4°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Refractive Index:
-42 ° (C=3, MeOH)
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


(R)-1-Acetyl-3-hydroxypyrrolidine, also known as (R)-A3HP, is a valuable chiral building block in chemical synthesis. This compound plays a crucial role in asymmetric synthesis, as its unique structure provides stereochemical control in various chemical reactions. In organic chemistry, (R)-1-acetyl-3-hydroxypyrrolidine is widely utilized as a key intermediate for the preparation of enantiomerically pure compounds. Its chiral nature allows for the synthesis of complex molecules with high optical purity, making it a versatile tool in the pharmaceutical and agrochemical industries. One notable application of (R)-A3HP is in the synthesis of bioactive molecules, where precise control over stereochemistry is essential for achieving the desired biological activity. By incorporating (R)-1-acetyl-3-hydroxypyrrolidine into the synthesis route, chemists can efficiently access enantiomerically enriched compounds with potential therapeutic benefits.Overall, the use of (R)-1-acetyl-3-hydroxypyrrolidine in chemical synthesis enables chemists to engage in asymmetric transformations and stereoselective reactions, paving the way for the creation of structurally diverse and stereochemically enriched compounds for various applications.