1,2-Benzenediamine, 4,5-bis(octyloxy)-

Base Information

Chemical Name:1,2-Benzenediamine, 4,5-bis(octyloxy)-
CAS No.:86723-23-1
Molecular Formula:C22H40N2O2
Molecular Weight:364.572
Hs Code.:

Synonyms:1,2-Benzenediamine,4,5-bis(octyloxy);1,2-dioctyloxy-4,5-diaminobenzene;1,2-bis(octoxy)-3,4-diaminobenzene;4,5-bis(octyloxy)benzene-1,2-diamine;1,2-bis(octyloxy)-4,5-diaminobenzene;1,2-diamino-4,5-dioctyloxybenzene;4,5-dioctyloxy-1,2-phenylenediamine;

Suppliers and Price of 1,2-Benzenediamine, 4,5-bis(octyloxy)-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 1,2-Benzenediamine, 4,5-bis(octyloxy)-

Chemical Property:

Boiling Point:502.6±45.0 °C(Predicted)
PSA：70.50000
Density:0.977±0.06 g/cm3(Predicted)
LogP:7.49200

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 1,2-Benzenediamine, 4,5-bis(octyloxy)-

There total 7 articles about 1,2-Benzenediamine, 4,5-bis(octyloxy)- 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: 90.0%

: 156777-91-2
1,2-bis(octyloxy)-4,5-dinitrobenzene

: 86723-23-1
1,2-bis(octyloxy)-4,5-diaminobenzene

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethanol; for 6h; under 1520 Torr;
DOI:10.1021/jo035840l

Reference yield:

: 111-83-1
1-bromo-octane

: 86723-23-1
1,2-bis(octyloxy)-4,5-diaminobenzene

Guidance literature:: Multi-step reaction with 3 steps

1: 95 percent / potassium carbonate / acetone / 48 h / Heating

2: 63 percent / nitric acid; acetic acid / CH₂Cl₂; H₂O / 0 - 20 °C

3: 90 percent / hydrogen / Pd/C / ethanol / 6 h / 1520 Torr

With hydrogen; nitric acid; potassium carbonate; acetic acid; palladium on activated charcoal; In ethanol; dichloromethane; water; acetone;
DOI:10.1021/jo035840l

Reference yield:

: 4956-41-6
1,2-dioctyloxybenzene

: 86723-23-1
1,2-bis(octyloxy)-4,5-diaminobenzene

Guidance literature:: Multi-step reaction with 2 steps

1: 63 percent / nitric acid; acetic acid / CH₂Cl₂; H₂O / 0 - 20 °C

2: 90 percent / hydrogen / Pd/C / ethanol / 6 h / 1520 Torr

With hydrogen; nitric acid; acetic acid; palladium on activated charcoal; In ethanol; dichloromethane; water;
DOI:10.1021/jo035840l