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Key Documents

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D130206

Sigma-Aldrich

2,3-Dimethoxybenzaldehyde

98%

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About This Item

Fórmula lineal:
(CH3O)2C6H3CHO
Número de CAS:
86-51-1
Peso molecular:
166.17
Beilstein/REAXYS Number:
908264
EC Number:
201-677-7
MDL number:
MFCD00003309
UNSPSC Code:
12352100
PubChem Substance ID:
24893406
NACRES:
NA.22

Quality Level

100

assay

98%

form

crystals

bp

137 °C/12 mmHg (lit.)

mp

48-52 °C (lit.)

SMILES string

[H]C(=O)c1cccc(OC)c1OC

InChI

1S/C9H10O3/c1-11-8-5-3-4-7(6-10)9(8)12-2/h3-6H,1-2H3

InChI key

JIVGSHFYXPRRSZ-UHFFFAOYSA-N

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Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Yadong Li et al.
BMC biochemistry, 12, 30-30 (2011-06-01)
Structural comparison between bacterial CueO and fungal laccases has suggested that a charged residue Glu (E106) in CueO replaces the corresponding residue Phe in fungal laccases at the gate of the tunnel connecting type II copper to the protein surface
Jong H Kim et al.
Annals of clinical microbiology and antimicrobials, 10, 23-23 (2011-06-02)
Disruption of cellular antioxidation systems should be an effective method for control of fungal pathogens. Such disruption can be achieved with redox-active compounds. Natural phenolic compounds can serve as potent redox cyclers that inhibit microbial growth through destabilization of cellular
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
Jiang Yan et al.
Science advances, 6(45) (2020-11-08)
Phenol is an important commodity chemical in the industry, which is currently produced using fossil feedstocks. Here, we report a strategy to produce phenol from lignin by directly deconstructing Csp2-Csp3 and C-O bonds under mild conditions. It was found that

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