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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-(2-methoxyphenyl)pyrrolidine;hydrochloride

COc1ccccc1C1CNCC1.Cl Request for Quotation
Chemical Name: 3-(2-methoxyphenyl)pyrrolidine;hydrochloride
CAS Number: 1106941-26-7
Product Number: AG00HBRC(AGN-PC-040QEZ)
Synonyms:
MDL No:
Molecular Formula: C11H16ClNO
Molecular Weight: 213.7038

Identification/Properties

Computed Properties
Molecular Weight:
213.705g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
213.092g/mol
Monoisotopic Mass:
213.092g/mol
Topological Polar Surface Area:
21.3A^2
Heavy Atom Count:
14
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-(2-Methoxyphenyl)pyrrolidine hydrochloride, also known as "name," is a versatile chemical compound commonly employed in chemical synthesis for its unique properties and applications. In the realm of chemical synthesis, 3-(2-Methoxyphenyl)pyrrolidine hydrochloride serves as a valuable intermediate in the preparation of various organic compounds. Its structural composition lends itself well to reactions involving nucleophiles, thereby enabling the formation of complex molecules through diverse synthetic routes. Furthermore, the presence of the pyrrolidine moiety confers specific stereochemical characteristics to the compound, which can be strategically leveraged in the synthesis of chiral molecules. This aspect is particularly advantageous in the pharmaceutical industry, where enantiomerically pure compounds often exhibit distinct biological activities.With its versatile utility and structural features, 3-(2-Methoxyphenyl)pyrrolidine hydrochloride plays a crucial role in the development of novel compounds and synthetic strategies, making it an indispensable tool in the field of chemical synthesis.