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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)-

(R)-2-(Methoxydiphenylmethyl)pyrrolidine

COC(c1ccccc1)(c1ccccc1)[C@H]1CCCN1 Request for Quotation
Chemical Name: (R)-2-(Methoxydiphenylmethyl)pyrrolidine
CAS Number: 948595-05-9
Product Number: AG006RB2(AGN-PC-0ONZHZ)
Synonyms:
MDL No: MFCD09750441
Molecular Formula: C18H21NO
Molecular Weight: 267.3654

Identification/Properties

Properties
Storage:
2-8℃;
Computed Properties
Molecular Weight:
267.372g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
4
Exact Mass:
267.162g/mol
Monoisotopic Mass:
267.162g/mol
Topological Polar Surface Area:
21.3A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
274
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)-2-(Methoxydiphenylmethyl) pyrrolidine is a versatile compound widely used in chemical synthesis for its unique properties. This compound serves as a valuable chiral building block in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. It plays a crucial role in asymmetric synthesis, allowing chemists to selectively produce enantiomerically pure compounds with high efficiency.In chemical synthesis, (R)-2-(Methoxydiphenylmethyl) pyrrolidine is often employed as a chiral auxiliary or a ligand in catalytic reactions. Its asymmetric nature enables the control of stereochemistry in organic reactions, facilitating the creation of complex molecular structures with desired stereochemical outcomes. Additionally, this compound can be utilized in the synthesis of natural products and biologically active molecules where chirality plays a significant role in determining their pharmacological properties.Furthermore, (R)-2-(Methoxydiphenylmethyl) pyrrolidine exhibits good stability and compatibility with a variety of reaction conditions, making it a preferred choice for chemists seeking to perform enantioselective transformations. Its utility in various chemical transformations underscores its importance in the field of organic chemistry and highlights its potential to enable the efficient production of optically pure compounds for diverse applications.