3-Hydroxy-4-(methylamino)benzaldehyde

Base Information

Chemical Name:3-Hydroxy-4-(methylamino)benzaldehyde
CAS No.:54903-56-9
Molecular Formula:C8H9NO2
Molecular Weight:151.1626
Hs Code.:
DSSTox Substance ID:DTXSID60203419

Synonyms:3-Hydroxy-4-(methylamino)benzaldehyde;JPB 35;Benzaldehyde, 3-hydroxy-4-(methylamino)-;54903-56-9;BRN 2087376;SCHEMBL15982258;DTXSID60203419;MB01978;LS-25074

Suppliers and Price of 3-Hydroxy-4-(methylamino)benzaldehyde

Supply Marketing:

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

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Chemical Property of 3-Hydroxy-4-(methylamino)benzaldehyde

Chemical Property:

Vapor Pressure:0.000717mmHg at 25°C
Boiling Point:298.4°Cat760mmHg
Flash Point:134.3°C
Density:1.27g/cm³
XLogP3:1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:151.063328530
Heavy Atom Count:11
Complexity:138

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CNC1=C(C=C(C=C1)C=O)O

Technology Process of 3-Hydroxy-4-(methylamino)benzaldehyde

There total 3 articles about 3-Hydroxy-4-(methylamino)benzaldehyde 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:

: 54903-66-1
2,3-dihydro-3-methyl-2-oxobenzo[d]oxazole-6-carbaldehyde

: 54903-56-9
3-hydroxy-4-methylaminobenzaldehyde

Guidance literature:: With sodium hydroxide; for 4h; Heating;
DOI:10.1135/cccc19970494

Reference yield:

: 21892-80-8
3-methylbenzo[d]oxazol-2(3H)-one

: 54903-56-9
3-hydroxy-4-methylaminobenzaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / trifluoroacetic acid / 20 h / Heating

2: aq. NaOH / 4 h / Heating

With sodium hydroxide; trifluoroacetic acid;
DOI:10.1135/cccc19970494