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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)-

Pyrrolidine, 2-[(4-methoxyphenyl)methyl]-

COc1ccc(cc1)CC1CCCN1 Request for Quotation
Chemical Name: Pyrrolidine, 2-[(4-methoxyphenyl)methyl]-
CAS Number: 66162-38-7
Product Number: AG006JGP(AGN-PC-0LKSI5)
Synonyms:
MDL No: MFCD02663425
Molecular Formula: C12H17NO
Molecular Weight: 191.2695

Identification/Properties

Computed Properties
Molecular Weight:
191.274g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
191.131g/mol
Monoisotopic Mass:
191.131g/mol
Topological Polar Surface Area:
21.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
164
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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


2-(4-Methoxybenzyl)pyrrolidine is a valuable chemical compound utilized in various organic synthesis processes. This versatile compound serves as a key building block in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure and reactivity make it a crucial component in the creation of complex molecules with diverse applications. Whether it is used as a chiral auxiliary, a protecting group, or a precursor for heterocyclic compounds, 2-(4-Methoxybenzyl)pyrrolidine plays a vital role in the advancement of modern chemical synthesis techniques. Its presence in the toolkit of synthetic chemists enables the efficient construction of intricate molecular structures and paves the way for the development of new materials and compounds with significant potential in various industries.