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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, 3-(2-methoxyphenyl)-

COc1ccccc1C1CNCC1 Request for Quotation
Chemical Name: Pyrrolidine, 3-(2-methoxyphenyl)-
CAS Number: 91246-24-1
Product Number: AG006DBT(AGN-PC-003F6T)
Synonyms:
MDL No:
Molecular Formula: C11H15NO
Molecular Weight: 177.2429

Identification/Properties

Properties
BP:
275.3±33.0°C at 760 mmHg
Storage:
2-8℃;Light sensitive;
Form:
Solid
Computed Properties
Molecular Weight:
177.247g/mol
XLogP3:
1.6
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:
21.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
160
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-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


3-(2-Methoxyphenyl)pyrrolidine, a versatile chemical compound, finds wide application in organic synthesis. As a key intermediate in the pharmaceutical industry, it is utilized in the preparation of various medicinally important compounds. Its unique structure and reactive properties make it a valuable building block for the synthesis of complex molecules, particularly those with significant biological activity. Additionally, 3-(2-Methoxyphenyl)pyrrolidine serves as a crucial reagent in the development of novel drugs, agrochemicals, and materials due to its ability to undergo various chemical transformations. Its role in the creation of diverse molecular structures highlights its importance in advancing the field of chemical synthesis.