2-benzyl-4-bromoisoindoline hydrochloride

Base Information

Chemical Name:2-benzyl-4-bromoisoindoline hydrochloride
CAS No.:923590-92-5
Molecular Formula:C₁₅H₁₄BrN*ClH
Molecular Weight:324.648
Hs Code.:

Synonyms:2-benzyl-4-bromoisoindoline hydrochloride

Suppliers and Price of 2-benzyl-4-bromoisoindoline hydrochloride

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
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price

Total 1 raw suppliers

Chemical Property of 2-benzyl-4-bromoisoindoline hydrochloride

Chemical Property:

Purity/Quality:: 95%-98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-benzyl-4-bromoisoindoline hydrochloride

There total 4 articles about 2-benzyl-4-bromoisoindoline hydrochloride 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:

: 923590-78-7
2-benzyl-4-bromoisoindoline

: 923590-92-5
2-benzyl-4-bromoisoindoline hydrochloride

Guidance literature:: With hydrogenchloride; In methanol; Product distribution / selectivity;

Reference yield:

: 127168-82-5
3-bromo-1,2-bis(bromomethyl)benzene

: 100-46-9
benzylamine

: 923590-92-5
2-benzyl-4-bromoisoindoline hydrochloride

Guidance literature:: 3-bromo-1,2-bis(bromomethyl)benzene; benzylamine; With potassium hydrogencarbonate; In acetonitrile; at 20 - 80 ℃; for 20h;

With potassium carbonate; In water; ethyl acetate; pH=> 9;

With hydrogenchloride; In methanol; ethanol; tert-butyl methyl ether; at 0 ℃; for 15h; Product distribution / selectivity;

Reference yield:

: 576-23-8
2,3-dimethylbromobenzene

: 923590-92-5
2-benzyl-4-bromoisoindoline hydrochloride

Guidance literature:: Multi-step reaction with 3 steps

1: N-Bromosuccinimide / dibenzoyl peroxide / tetrachloromethane / 15 h / Reflux; Inert atmosphere

2: potassium hydrogensulfate / acetonitrile / 17 h / 77 - 80 °C

3: hydrogenchloride / methanol

With hydrogenchloride; potassium hydrogensulfate; N-Bromosuccinimide; dibenzoyl peroxide; In methanol; tetrachloromethane; acetonitrile;