365564
Methyl 4-methoxy-2-indolecarboxylate
99%
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About This Item
Formula empirica (notazione di Hill):
C11H11NO3
Numero CAS:
Peso molecolare:
205.21
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Saggio
99%
Punto di fusione
140-142 °C (lit.)
Stringa SMILE
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
GLCZQTLCVLVFGV-UHFFFAOYSA-N
Descrizione generale
Methyl 4-methoxy-2-indolecarboxylate is an indole derivative.
Applicazioni
- 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). 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.
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Certificati d'analisi (COA)
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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
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
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