| Identification | More | [Name]
Methyl indole-5-carboxylate | [CAS]
1011-65-0 | [Synonyms]
INDOLE-5-CARBOXYLIC ACID METHYL ESTER
LABOTEST-BB LT00454878
METHYL 1H-INDOLE-5-CARBOXYLATE
METHYL INDOLE-5-CABOXYLATE
METHYL INDOLE-5-CARBOXYLATE
RARECHEM AH BS 0114
1H-Indole-5-carboxylicacidmethylester
5-IndolecarboxylicAcidAcidMethylEster
Methyl indole-5-carboxylate, 98+%
Mehtyl 1H-indole-5-carboxylate | [EINECS(EC#)]
627-947-8 | [Molecular Formula]
C10H9NO2 | [MDL Number]
MFCD00153023 | [Molecular Weight]
175.18 | [MOL File]
1011-65-0.mol |
| Chemical Properties | Back Directory | [Appearance]
White to tan crystalline powder | [Melting point ]
126-128 °C (lit.) | [Boiling point ]
331.7±15.0 °C(Predicted) | [density ]
1.253±0.06 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Inert atmosphere,Room temperature | [solubility ]
soluble in Chloroform, Methanol | [form ]
powder to crystal | [pka]
16.09±0.30(Predicted) | [color ]
White to Gray to Brown | [Water Solubility ]
Insoluble in water. | [BRN ]
474256 | [CAS DataBase Reference]
1011-65-0(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [HazardClass ]
IRRITANT | [HS Code ]
29339900 |
| Hazard Information | Back Directory | [Chemical Properties]
White to tan crystalline powder | [Uses]
Methyl indole-5-carboxylate may be used as a reactant in the following processes:
- biosynthesis of inhibitors of protein kinases
- metal-free Friedel-Crafts alkylation
- preparation of diphenylsulfonium ylides from Martin′s sulfurane
- cross dehydrogenative coupling reactions
- synthesis of indirubin derivatives
- preparation of aminoindolylacetates
| [Definition]
ChEBI: Methyl indole-5-carboxylate is an indolyl carboxylic acid. | [General Description]
Methyl indole-5-carboxylate (Methyl 1H-indole-5-carboxylate), a substituted 1H-indole, can be prepared by the esterification of indole-5-carboxylic acid. Its efficacy as a substrate for indigoid generation has been assessed. |
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