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Merck
CN

292508

2,6-二甲氧基苯甲醛

99%

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关于此项目

线性分子式:
(CH3O)2C6H3CHO
化学文摘社编号:
分子量:
166.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
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产品名称

2,6-二甲氧基苯甲醛, 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.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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历史批次信息供参考:

分析证书(COA)

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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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