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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)-

3-Pyrrolidinol, 1-(phenylmethyl)-, (3R)-

O[C@@H]1CCN(C1)Cc1ccccc1 Request for Quotation
Chemical Name: 3-Pyrrolidinol, 1-(phenylmethyl)-, (3R)-
CAS Number: 101930-07-8
Product Number: AG0005Z6(AGN-PC-0NVB08)
Synonyms:
MDL No: MFCD00075484
Molecular Formula: C11H15NO
Molecular Weight: 177.2429

Identification/Properties

Properties
MP:
212 °C
BP:
116°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Liquid
Refractive Index:
n20/D 1.548(lit.)
Computed Properties
Molecular Weight:
177.247g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
177.115g/mol
Monoisotopic Mass:
177.115g/mol
Topological Polar Surface Area:
23.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
154
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#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (R)-3-Hydroxy-1-benzylpyrrolidine is a chiral building block that plays a crucial role in chemical synthesis. Due to its unique structure and stereochemistry, it serves as a valuable intermediate in the preparation of various pharmaceutical compounds and natural products. Its presence in organic reactions can enable the creation of asymmetric centers, making it a versatile tool in the synthesis of complex molecules.In organic chemistry, (R)-3-Hydroxy-1-benzylpyrrolidine is often utilized as a key starting material for the construction of biologically active compounds, such as chiral drugs and agrochemicals. Its chiral nature allows for the creation of enantiopure products, which is essential in drug development to ensure specific interactions with biological targets and minimize side effects.The application of (R)-3-Hydroxy-1-benzylpyrrolidine extends to various important transformations, including asymmetric catalysis, stereoselective reductions, and carbon-carbon bond formation reactions. By incorporating this compound into synthetic pathways, chemists can access a wide range of structurally diverse molecules with high levels of stereocontrol.Overall, (R)-3-Hydroxy-1-benzylpyrrolidine serves as a valuable building block in chemical synthesis, enabling the efficient and selective construction of complex molecules with specific chirality, ultimately contributing to the advancement of pharmaceutical and organic chemistry research.