A-BROMO-4-NITROACETOPHENONE HEXAMINE

Base Information

Chemical Name:A-BROMO-4-NITROACETOPHENONE HEXAMINE
CAS No.:91147-75-0
Molecular Formula:C14H18BrN5O3
Molecular Weight:384.233
Hs Code.:
Mol file:91147-75-0.mol

Synonyms:A-BROMO-4-NITROACETOPHENONE HEXAMINE;2-Bromo-1-(4-nitrophenyl)ethanone compound with 1,3,5,7-tetraazatricyclo[3.3.1.1./3.7]decane;伪-Bromo-4-nitroacetophenone hexamine

Suppliers and Price of A-BROMO-4-NITROACETOPHENONE HEXAMINE

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 4 raw suppliers

Chemical Property of A-BROMO-4-NITROACETOPHENONE HEXAMINE

Chemical Property:

PSA：75.85000
LogP:1.42740

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of A-BROMO-4-NITROACETOPHENONE HEXAMINE

There total 1 articles about A-BROMO-4-NITROACETOPHENONE HEXAMINE 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:

: 100-97-0
hexamethylenetetramine

: 99-81-0
4-Nitrophenacyl bromide

: 91147-75-0
C₈H₆BrNO₃*C₆H₁₂N₄

Guidance literature:: In chloroform; at 20 ℃; for 24h;
DOI:10.1016/j.ejmech.2013.04.022

Reference yield: 80.0%

: 91147-75-0
C₈H₆BrNO₃*C₆H₁₂N₄

: 5425-81-0
2-amino-1-(4-nitrophenyl)ethanone hydrochloride

Guidance literature:: With hydrogenchloride; In ethanol; chloroform; at 20 ℃; for 72h;
DOI:10.1016/j.ejmech.2013.04.022

Reference yield:

: 91147-75-0
C₈H₆BrNO₃*C₆H₁₂N₄

: 1456532-36-7
2-amino-1-(4-nitro)acetophenone thiosemicarbazone

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogenchloride / ethanol; chloroform / 72 h / 20 °C

2: acetic acid / ethanol / 24 h / 20 °C

With hydrogenchloride; acetic acid; In ethanol; chloroform;
DOI:10.1016/j.ejmech.2013.04.022