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D130206

Sigma-Aldrich

2,3-Dimethoxybenzaldehyde

98%

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About This Item

Fórmula linear:
(CH3O)2C6H3CHO
Número CAS:
86-51-1
Peso molecular:
166.17
Beilstein:
908264
Número CE:
201-677-7
Número MDL:
MFCD00003309
Código UNSPSC:
12352100
ID de substância PubChem:
24893406
NACRES:
NA.22

Ensaio

98%

forma

crystals

pb

137 °C/12 mmHg (lit.)

pf

48-52 °C (lit.)

cadeia de caracteres SMILES

[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

chave InChI

JIVGSHFYXPRRSZ-UHFFFAOYSA-N

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Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

235.4 °F - closed cup

Ponto de fulgor (°C)

113 °C - closed cup

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

Certificados de análise (COA)

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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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