3,4-Dihydroxy-2-nitrobenzaldehyde

Base Information

Chemical Name:3,4-Dihydroxy-2-nitrobenzaldehyde
CAS No.:50545-37-4
Molecular Formula:C7H5NO5
Molecular Weight:183.12
Hs Code.:2913000090
ChEMBL ID:CHEMBL139882
DSSTox Substance ID:DTXSID60564633
Nikkaji Number:J522.466G
Wikidata:Q82449405
Mol file:50545-37-4.mol

Synonyms:3,4-DIHYDROXY-2-NITROBENZALDEHYDE;50545-37-4;CHEMBL139882;Benzaldehyde, 3,4-dihydroxy-2-nitro-;SCHEMBL9448642;DTXSID60564633;BCP29688;3,4-Dihydroxy-2-nitro-benzaldehyde;BDBM50004049;AKOS006228336;CS-0262006;EN300-8085153

Suppliers and Price of 3,4-Dihydroxy-2-nitrobenzaldehyde

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
3,4-Dihydroxy-2-nitrobenzaldehyde
2.5g
$ 300.00

Biosynth Carbosynth
3,4-Dihydroxy-2-nitrobenzaldehyde
25 g
$ 500.00

Biosynth Carbosynth
3,4-Dihydroxy-2-nitrobenzaldehyde
10 g
$ 275.00

Biosynth Carbosynth
3,4-Dihydroxy-2-nitrobenzaldehyde
5 g
$ 175.00

Biosynth Carbosynth
3,4-Dihydroxy-2-nitrobenzaldehyde
2 g
$ 95.00

Biosynth Carbosynth
3,4-Dihydroxy-2-nitrobenzaldehyde
1 g
$ 62.50

Total 5 raw suppliers

Chemical Property of 3,4-Dihydroxy-2-nitrobenzaldehyde

Chemical Property:

PSA：103.35000
LogP:1.34170
Storage Temp.:Amber Vial, Refrigerator, under inert atmosphere
Solubility.:DMSO (Slightly), Methanol (Slightly)
XLogP3:1.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:1
Exact Mass:183.01677226
Heavy Atom Count:13
Complexity:213

Purity/Quality:

99% ^*data from raw suppliers

3,4-Dihydroxy-2-nitrobenzaldehyde ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=C(C(=C1C=O)[N+](=O)[O-])O)O

Technology Process of 3,4-Dihydroxy-2-nitrobenzaldehyde

There total 6 articles about 3,4-Dihydroxy-2-nitrobenzaldehyde 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: 92.0%

: 2450-26-2
2-nitrovanillin

: 50545-37-4
3,4-dihydroxy-2-nitrobenzaldehyde

Guidance literature:: With boron tribromide; In dichloromethane; at -78 ℃;
DOI:10.1016/S0040-4039(00)97054-0

Reference yield:

: 6284-92-0
3-hydroxy-4-methoxy-2-nitrobenzaldehyde

: 50545-37-4
3,4-dihydroxy-2-nitrobenzaldehyde

Guidance literature:: With pyridine; aluminum (III) chloride; In chloroform; Reflux;
DOI:10.1016/j.bmcl.2014.08.024

Reference yield:

: 621-59-0
isovanillin

: 50545-37-4
3,4-dihydroxy-2-nitrobenzaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1: nitric acid / acetic anhydride

2: aluminum (III) chloride; pyridine / chloroform / Reflux

With pyridine; aluminum (III) chloride; nitric acid; In chloroform; acetic anhydride;
DOI:10.1016/j.bmcl.2014.08.024