292508
2,6-Dimethoxybenzaldehyde
99%
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About This Item
Linear Formula:
(CH3O)2C6H3CHO
CAS Number:
Molecular Weight:
166.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Product Name
2,6-Dimethoxybenzaldehyde, 99%
InChI
1S/C9H10O3/c1-11-8-4-3-5-9(12-2)7(8)6-10/h3-6H,1-2H3
SMILES string
COc1cccc(OC)c1C=O
InChI key
WXSGQHKHUYTJNB-UHFFFAOYSA-N
assay
99%
form
solid
bp
285 °C (lit.)
mp
96-98 °C (lit.)
functional group
aldehyde
Application
2,6-Dimethoxybenzaldehyde has been used in the preparation of 2,6-dihydroxybenzaldehyde by demethylation with AlBr3.
General description
Demethylation of 2,6-dimethoxybenzaldehydes with magnesium iodide etherate has been studied.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Regioselective demethylation of 2, 6-dimethoxybenzaldehydes with magnesium iodide etherate.
Yamaguchi S, et al.
Tetrahedron Letters, 40(41), 7363-7365 (1999)
Synthesis of facially-encumbered porphyrins. An approach to light-harvesting antenna complexes.
Wagner RW, et al.
Tetrahedron Letters, 32(14), 1703-1706 (1991)
Olga V Kupriyanova et al.
Drug testing and analysis, 12(8), 1154-1170 (2020-05-18)
N-(2-Methoxybenzyl)-2,5-dimethoxyphenethylamines (NBOMes) are synthetic phenethylamine derivatives emerging on the global drug market and reported to be associated with untoward effects in people who use drugs. Its action involves agonism at serotonin 5-HT2A receptors, affecting cognitive and behavioral processes. However, certain
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