1-(2-Phenylethenyl)pyrrolidine

Base Information

Chemical Name:1-(2-Phenylethenyl)pyrrolidine
CAS No.:6908-73-2
Molecular Formula:C₁₂H₁₅N
Molecular Weight:173.258
Hs Code.:
DSSTox Substance ID:DTXSID20709422

Synonyms:1-(2-Phenylethenyl)pyrrolidine;6908-73-2;beta-pyrrolidinostyrene;DTXSID20709422;OMRYFORMTXHEKG-UHFFFAOYSA-N

Suppliers and Price of 1-(2-Phenylethenyl)pyrrolidine

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 2 raw suppliers

Chemical Property of 1-(2-Phenylethenyl)pyrrolidine

Chemical Property:

XLogP3:3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:173.120449483
Heavy Atom Count:13
Complexity:162

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CCN(C1)C=CC2=CC=CC=C2

Technology Process of 1-(2-Phenylethenyl)pyrrolidine

There total 21 articles about 1-(2-Phenylethenyl)pyrrolidine 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%

: 123-75-1
pyrrolidine

: 122-78-1
phenylacetaldehyde

: 6908-73-2,13294-34-3
(E)-1-styrylpyrrolidine

Guidance literature:: In dichloromethane; at 25 ℃; for 15h; Molecular sieve; Inert atmosphere;
DOI:10.1021/jacs.0c09775

Reference yield: 92.0%

: 3389-53-5
phenylacetylpyrrolidine

: 13294-34-3,6908-73-2
2-phenyl-1-(1-pyrrolidinyl)ethene

Guidance literature:: With 1,1,3,3-Tetramethyldisiloxane; molybdenum hexacarbonyl; In ethyl acetate; at 65 ℃; for 0.25h; Temperature; chemoselective reaction;
DOI:10.1021/acscatal.7b00095