4,5-Diethoxybenzene-1,2-diamine

Base Information

Chemical Name:4,5-Diethoxybenzene-1,2-diamine
CAS No.:86723-14-0
Molecular Formula:C10H16N2O2
Molecular Weight:196.24600
Hs Code.:
DSSTox Substance ID:DTXSID90561872
Nikkaji Number:J2.772.257A
Wikidata:Q82445783
Mol file:86723-14-0.mol

Synonyms:4,5-Diethoxybenzene-1,2-diamine;86723-14-0;1,2-Benzenediamine, 4,5-diethoxy-;SCHEMBL8503295;DTXSID90561872

Suppliers and Price of 4,5-Diethoxybenzene-1,2-diamine

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

TRC
1,2-Diamino-4,5-ethoxybenzene,Hydrochloride
100mg
$ 130.00

American Custom Chemicals Corporation
1,2-DIAMINO-4,5-ETHOXYBENZENE HYDROCHLORIDE 95.00%
1G
$ 1593.90

American Custom Chemicals Corporation
1,2-DIAMINO-4,5-ETHOXYBENZENE HYDROCHLORIDE 95.00%
100MG
$ 716.10

Total 4 raw suppliers

Chemical Property of 4,5-Diethoxybenzene-1,2-diamine

Chemical Property:

PSA：70.50000
LogP:2.81080
Solubility.:Methanol, Water,
XLogP3:1.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:196.121177757
Heavy Atom Count:14
Complexity:148

Purity/Quality:

99% ^*data from raw suppliers

1,2-Diamino-4,5-ethoxybenzene,Hydrochloride ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC1=C(C=C(C(=C1)N)N)OCC
Uses Reacts with aldehydes to produce highly fluorescent benzimidazole derivatives. 1,2-Diamino-4,5-ethoxybenzene, Hydrochloride can be used for the detection of aromatic aldehydes as well as DTAN Reacts with aldehydes to produce highly fluorescent benzimidazole derivatives. Can be used for the detection of aromatic aldehydes as well as DTAN.

Technology Process of 4,5-Diethoxybenzene-1,2-diamine

There total 2 articles about 4,5-Diethoxybenzene-1,2-diamine 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:

: 40294-27-7
1,2-diethoxy-4,5-dinitrobenzene

: 86723-14-0
1,2-diethoxy-4,5-diaminobenzene

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethyl acetate;
DOI:10.1016/0040-4039(95)01562-V

Reference yield:

: 2050-46-6
1,2-diethoxybenzene

: 86723-14-0
1,2-diethoxy-4,5-diaminobenzene

Guidance literature:: Multi-step reaction with 2 steps

1: 95 percent / 70percent HNO₃ / 80 °C

2: H₂ / Pd/C / ethyl acetate

With hydrogen; nitric acid; palladium on activated charcoal; In ethyl acetate;
DOI:10.1016/0040-4039(95)01562-V