N-[(S)-1-Phenylethyl]-4-methoxyaniline

Base Information

Chemical Name:N-[(S)-1-Phenylethyl]-4-methoxyaniline
CAS No.:156092-13-6
Molecular Formula:C₁₅H₁₇NO
Molecular Weight:227.306
Hs Code.:
DSSTox Substance ID:DTXSID001225821
Nikkaji Number:J1.337.226H

Synonyms:SCHEMBL15004002;DTXSID001225821;N-[(S)-1-Phenylethyl]-4-methoxyaniline;(alphaS)-N-(4-Methoxyphenyl)-alpha-methylbenzenemethanamine;156092-13-6

Suppliers and Price of N-[(S)-1-Phenylethyl]-4-methoxyaniline

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of N-[(S)-1-Phenylethyl]-4-methoxyaniline

Chemical Property:

XLogP3:3.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:227.131014166
Heavy Atom Count:17
Complexity:205

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C1=CC=CC=C1)NC2=CC=C(C=C2)OC
Isomeric SMILES:C[C@@H](C1=CC=CC=C1)NC2=CC=C(C=C2)OC

Technology Process of N-[(S)-1-Phenylethyl]-4-methoxyaniline

There total 25 articles about N-[(S)-1-Phenylethyl]-4-methoxyaniline which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 99.0%

: 2743-00-2
4-methoxy-N-(1-phenylethylidene)aniline

: 156092-13-6
(S)-4-methoxy-N-(1-phenylethyl)aniline

Guidance literature:: 4-methoxy-N-(1-phenylethylidene)aniline; With (S)-1-pivaloyl-2-(phenylcarbamoyl)pyrrolidine; trichlorosilane; In dichloromethane; at 0 ℃; for 24h; Inert atmosphere;

With sodium hydrogencarbonate; In dichloromethane; optical yield given as %ee; enantioselective reaction; Inert atmosphere;
DOI:10.1016/j.tet.2012.03.035

Reference yield: 99.0%

: 2743-00-2,125231-22-3
(E)-4-methoxy-N-(1-phenylethylidene)benzenamine

: 2743-01-3,126522-56-3
(R)-N-(4-methoxyphenyl)-(1-phenylethyl)amine

: 156092-13-6
(S)-4-methoxy-N-(1-phenylethyl)aniline

Guidance literature:: With Dimethylphenylsilane; C₉₂H₁₀₆; bis(pentafluorophenyl)borohydride; at 0 ℃; for 8h; Temperature; Reagent/catalyst; Solvent; Time; enantioselective reaction; Schlenk technique; Glovebox;
DOI:10.1039/c4ob02419b

Reference yield: 96.0%

: 2743-00-2,125231-22-3
(E)-4-methoxy-N-(1-phenylethylidene)benzenamine

: 156092-13-6
(S)-4-methoxy-N-(1-phenylethyl)aniline

Guidance literature:: With trichlorosilane; [(S)-2-(hydroxydiphenylmethyl)-pyrrolidin-1-yl]-(1-methyl-1H-imidazol-2-yl)methanone; In dichloromethane; at 0 ℃; for 4h; Product distribution / selectivity;