365564
Methyl 4-methoxy-2-indolecarboxylate
99%
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1 G
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1 G
R$ 1.056,00
About This Item
Fórmula empírica (Notação de Hill):
C11H11NO3
Número CAS:
Peso molecular:
205.21
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
Nível de qualidade
Ensaio
99%
pf
140-142 °C (lit.)
grupo funcional
ester
cadeia de caracteres SMILES
COC(=O)c1cc2c(OC)cccc2[nH]1
InChI
1S/C11H11NO3/c1-14-10-5-3-4-8-7(10)6-9(12-8)11(13)15-2/h3-6,12H,1-2H3
chave InChI
GLCZQTLCVLVFGV-UHFFFAOYSA-N
Categorias relacionadas
Descrição geral
Methyl 4-methoxy-2-indolecarboxylate is an indole derivative.[1]
Aplicação
- reactant in [3+2] annulation reactions
- reactant in preparation of inhibitors of mammalian secreted phospholipases A2
- reactant in Heck reactions
- reactant in preparation of indole fatty alcohol derivatives
- reactant in methylation reactions
Methyl 4-methoxy-2-indolecarboxylate is suitable for use in the production of dyes by Escherichia coli expressing naphthalene dioxygenase (NDO) and toluene dioxygenase (TDO).[1] It is also suitable for use in the production of dyes by E. coli expressing multicomponent phenol hydroxylase (mPH) from Pseudomonas sp. strains KL33 and KL28.[2]
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
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J Y Kim et al.
Letters in applied microbiology, 41(2), 163-168 (2005-07-22)
To establish multicomponent phenol hydroxylases (mPHs) as novel biocatalysts for producing dyestuffs and hydroxyindoles such as 7-hydroxyindole (7-HI) from indole and its derivatives. We have isolated Pseudomonas sp. KL33, which possesses a phenol degradation pathway similar to that found in
J Y Kim et al.
Letters in applied microbiology, 36(6), 343-348 (2003-05-20)
To isolate and characterize the phorate [O,O-diethyl-S-(ethylthio)methyl phosphoradiothioate] degrading bacteria from agricultural soil, and their assessment for multifarious biological activities of environmental and agronomic significance. Based on their morphological and biochemical characteristics, the selected isolates PS-1, PS-2 and PS-3 were
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