benzoisoquinolinium dibenzoylmethylid

Base Information

Chemical Name:benzoisoquinolinium dibenzoylmethylid
CAS No.:75052-20-9
Molecular Formula:C₂₈H₁₉NO₂
Molecular Weight:401.464
Hs Code.:

benzo<g>isoquinolinium dibenzoylmethylid

Synonyms:

Suppliers and Price of benzoisoquinolinium dibenzoylmethylid

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 0 raw suppliers

Chemical Property of benzoisoquinolinium dibenzoylmethylid

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of benzoisoquinolinium dibenzoylmethylid

There total 3 articles about benzoisoquinolinium dibenzoylmethylid 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: 70.0%

: 75052-15-2
2-phenacylbenzoisoquinolinium bromide

: 98-88-4
benzoyl chloride

: 75052-20-9
benzoisoquinolinium dibenzoylmethylid

Guidance literature:: With triethylamine; In chloroform; for 1h;
DOI:10.1007/BF00553704

Reference yield:

: 260-32-2
2-azaanthracene

: 75052-20-9
benzoisoquinolinium dibenzoylmethylid

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / acetonitrile / 2 h / Heating

2: 70 percent / triethylamine / CHCl₃ / 1 h

With triethylamine; In chloroform; acetonitrile;
DOI:10.1007/BF00553704

Reference yield:

: 70-11-1
α-bromoacetophenone

: 75052-20-9
benzoisoquinolinium dibenzoylmethylid

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / acetonitrile / 2 h / Heating

2: 70 percent / triethylamine / CHCl₃ / 1 h

With triethylamine; In chloroform; acetonitrile;
DOI:10.1007/BF00553704