Methanone, [3-chloro-4-(1-pyrrolidinyl)phenyl]phenyl-

Base Information

Chemical Name:Methanone, [3-chloro-4-(1-pyrrolidinyl)phenyl]phenyl-
CAS No.:834895-53-3
Molecular Formula:C₁₇H₁₆ClNO
Molecular Weight:285.773
Hs Code.:
DSSTox Substance ID:DTXSID30479361

Synonyms:834895-53-3;Methanone, [3-chloro-4-(1-pyrrolidinyl)phenyl]phenyl-;DTXSID30479361

Suppliers and Price of Methanone, [3-chloro-4-(1-pyrrolidinyl)phenyl]phenyl-

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 1 raw suppliers

Chemical Property of Methanone, [3-chloro-4-(1-pyrrolidinyl)phenyl]phenyl-

Chemical Property:

XLogP3:4.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:285.0920418
Heavy Atom Count:20
Complexity:334

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CCN(C1)C2=C(C=C(C=C2)C(=O)C3=CC=CC=C3)Cl

Technology Process of Methanone, [3-chloro-4-(1-pyrrolidinyl)phenyl]phenyl-

There total 3 articles about Methanone, [3-chloro-4-(1-pyrrolidinyl)phenyl]phenyl- 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: 71.0%

: 123-75-1
pyrrolidine

: 6284-79-3
3,4-dichlorobenzophenone

: 834895-53-3
3-chloro-4-pyrrolidinobenzophenone

Guidance literature:: Heating;
DOI:10.1016/j.tet.2004.10.069

Reference yield:

: 51-44-5
3,4-dichlorbenzoic acid

: 834895-53-3
3-chloro-4-pyrrolidinobenzophenone

Guidance literature:: Multi-step reaction with 3 steps

1: thionyl chloride; N,N-dimethylformamide / 2 h / Heating

2: 54 percent / AlCl₃ / 1 h / Heating

3: 71 percent / Heating

With aluminium trichloride; thionyl chloride; N,N-dimethyl-formamide; 2: Friedel-Crafts acylation;
DOI:10.1016/j.tet.2004.10.069

Reference yield:

: 3024-72-4
3,4-dichlorobenzoyl chloride

: 834895-53-3
3-chloro-4-pyrrolidinobenzophenone

Guidance literature:: Multi-step reaction with 2 steps

1: 54 percent / AlCl₃ / 1 h / Heating

2: 71 percent / Heating

With aluminium trichloride; 1: Friedel-Crafts acylation;
DOI:10.1016/j.tet.2004.10.069