Methyl 6-methoxy-1H-indole-2-carboxylate

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Names

[ CAS No. ]:
98081-83-5

[ Name ]:
Methyl 6-methoxy-1H-indole-2-carboxylate

[Synonym ]:
Methyl 6-methoxy-1H-indole-2-carboxylate
MFCD00134301
1H-Indole-2-carboxylic acid, 6-methoxy-, methyl ester

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Boiling Point ]:
370.1±22.0 °C at 760 mmHg

[ Melting Point ]:
117-119 °C(lit.)

[ Molecular Formula ]:
C11H11NO3

[ Molecular Weight ]:
205.210

[ Flash Point ]:
177.6±22.3 °C

[ Exact Mass ]:
205.073898

[ PSA ]:
51.32000

[ LogP ]:
2.33

[ Vapour Pressure ]:
0.0±0.8 mmHg at 25°C

[ Index of Refraction ]:
1.613

Safety Information

[ Hazard Codes ]:
Xi

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2933990090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • methyl 2-azido-3-(4-methoxyphenyl)prop-2-enoate
  • 4-Methoxybenzaldehyde
  • 2-Acetamidoacrylic acid
  • 1,2-Dibromo-4-methoxybenzene
  • Sodium Methylate
  • 3-(4-methoxy-2-nitrophenyl)acrylic acid methyl ester
  • 3-anisidine
  • Diethylphosphonoacetic acid

DownStream

  • 6-Hydroxyindole-2-carboxylic acid
  • 6-Methoxyindole
  • 1-(benzenesulfonyl)-6-methoxyindole-3-carbaldehyde
  • (6-Methoxy-1H-indol-2-yl)methanol
  • 6-Methoxy-1H-indole-2-carbaldehyde
  • 6-Methoxyindole-3-carboxaldehyde
  • methyl 6-hydroxy-1h-indole-2-carboxylate
  • Methyl 6-methoxy-1-methyl-1H-indole-2-carboxylate
  • 6-Methoxy-1H-indole-2-carboxylic acid
  • 6-Methoxy-2-methyl-1H-indole

Customs

[ HS Code ]: 2933990090

[ Summary ]:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Multicomponent phenol hydroxylase-catalysed formation of hydroxyindoles and dyestuffs from indole and its derivatives.

Lett. Appl. Microbiol. 41(2) , 163-8, (2005)

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 ...

Production of dyestuffs from indole derivatives by naphthalene dioxygenase and toluene dioxygenase.

Lett. Appl. Microbiol. 36(6) , 343-8, (2003)

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 ...


More Articles

Related Compounds

  • ethyl 6-methoxy-3-methyl-1H-indole-2-carboxylate
  • Methyl 6-methoxy-1-methyl-1H-indole-2-carboxylate
  • methyl 6-formamido-5-methoxy-1H-indole-2-carboxylate
  • methyl 6-acetamido-4-methoxy-1H-indole-2-carboxylate
  • methyl 5-benzyloxy-6-methoxy-1H-indole-2-carboxylate
  • Methyl 3-amino-6-methoxy-1H-indole-2-carboxylate
  • (1-Benzyl-4-phenylpyrrolidin-3-yl)methanamine hydrochloride
  • 3-(4-Fluorophenyl)-4-(methylthio)-1H-pyrrole-2,5-dione
  • 4-Bromo-7-fluoro-2-(trifluoromethyl)-1,3-benzoxazole
  • 3-Nitro-4-(trifluoromethoxy)benzyl bromide
  • 2-(1,6-Dihydro-6-oxo-2-pyridinyl)benzoic acid
  • 3-(2-Oxo-ethoxy)-azetidine-1-carboxylic acid tert-butyl ester
  • N-Boc-7-azidoheptan-1-amine
  • [1-methyl-3-(5-methyloxolan-2-yl)-1H-pyrazol-4-yl]methanol
  • 4-[(4H-1,2,4-Triazol-4-yl)methyl]piperidine hydrochloride
  • N-[2-(ethylamino)propyl]benzamide hydrochloride
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