Benzene, 1-methyl-2-nitro-4,5-bis(phenylmethoxy)-

Base Information

Chemical Name:Benzene, 1-methyl-2-nitro-4,5-bis(phenylmethoxy)-
CAS No.:4856-01-3
Molecular Formula:C21H19NO4
Molecular Weight:349.38000
Hs Code.:
Mol file:4856-01-3.mol

Synonyms:2-Nitro-4,5-bis-benzyloxy-toluol;4,5-dibenzyloxy-2-nitrotoluene;6-Nitro-3,4-dibenzyloxy-toluol;4,5-bis-benzyloxy-2-nitro-toluene;4,5-Bis-benzyloxy-2-nitro-toluol;

Suppliers and Price of Benzene, 1-methyl-2-nitro-4,5-bis(phenylmethoxy)-

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 Benzene, 1-methyl-2-nitro-4,5-bis(phenylmethoxy)-

Chemical Property:

Melting Point:98-100 °C
Boiling Point:523.4±45.0 °C(Predicted)
PSA：64.28000
Density:1.217±0.06 g/cm3(Predicted)
LogP:5.58440

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Benzene, 1-methyl-2-nitro-4,5-bis(phenylmethoxy)-

There total 3 articles about Benzene, 1-methyl-2-nitro-4,5-bis(phenylmethoxy)- 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:

: 100-39-0
benzyl bromide

: 452-86-8
4-methyl-1,2-dihydroxybenzene

: 4856-01-3
3,4-bis(benzyloxy)-6-nitrotoluene

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / N,N-dimethyl-formamide / 90 °C

2: acetic acid; nitric acid

With nitric acid; potassium carbonate; acetic acid; In N,N-dimethyl-formamide;
DOI:10.1039/c4tc01997k