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ChemicalBook > Product Catalogue >Organic Chemistry >Aldehydes >1-Methylindole-3-carboxaldehyde

1-Methylindole-3-carboxaldehyde

1-Methylindole-3-carboxaldehyde Structure
  • ₹4005 - ₹34564.23
  • Product name: 1-Methylindole-3-carboxaldehyde
  • CAS: 19012-03-4
  • MF: C10H9NO
  • MW: 159.18
  • EINECS:242-750-3
  • MDL Number:MFCD00014570
  • Synonyms:TIMTEC-BB SBB010057;RARECHEM AH BS 0121;1 METHYLINDOLE-3-ALDEHYDE;1-METHYLINDOLE-3-CARBALDEHYDE;1-METHYLINDOLE-3-CARBOXALDEHYDE;1-METHYL-1H-INDOLE-3-CARBOXALDEHYDE;AKOS JY2082515;N-Methylindole-3-Carboxaldehyde
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Brand

  • Sigma-Aldrich(India)
  • ottokemi

Package

  • 1gm
  • 5gm
  • 5G
  • 25gm
  • 25G
  • ManufacturerSigma-Aldrich(India)
  • Product number357987
  • Product description1-Methylindole-3-carboxaldehyde 97%
  • Packaging5G
  • Price₹10922.43
  • Updated2022-06-14
  • Buy
  • ManufacturerSigma-Aldrich(India)
  • Product number357987
  • Product description1-Methylindole-3-carboxaldehyde 97%
  • Packaging25G
  • Price₹34564.23
  • Updated2022-06-14
  • Buy
  • Manufacturerottokemi
  • Product number M 2093
  • Product description1-Methyl-3-formylindole 97%
  • Packaging1gm
  • Price₹4005
  • Updated2022-05-26
  • Buy
  • Manufacturerottokemi
  • Product number M 2093
  • Product description1-Methyl-3-formylindole 97%
  • Packaging5gm
  • Price₹9819
  • Updated2022-05-26
  • Buy
  • Manufacturerottokemi
  • Product number M 2093
  • Product description1-Methyl-3-formylindole 97%
  • Packaging25gm
  • Price₹30501
  • Updated2022-05-26
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
Sigma-Aldrich(India) 357987 1-Methylindole-3-carboxaldehyde 97% 5G ₹10922.43 2022-06-14 Buy
Sigma-Aldrich(India) 357987 1-Methylindole-3-carboxaldehyde 97% 25G ₹34564.23 2022-06-14 Buy
ottokemi M 2093 1-Methyl-3-formylindole 97% 1gm ₹4005 2022-05-26 Buy
ottokemi M 2093 1-Methyl-3-formylindole 97% 5gm ₹9819 2022-05-26 Buy
ottokemi M 2093 1-Methyl-3-formylindole 97% 25gm ₹30501 2022-05-26 Buy

Properties

Melting point :70-72 °C (lit.)
Boiling point :186-189 °C(Press: 3-4 Torr)
Density :1.10±0.1 g/cm3(Predicted)
storage temp. :Keep in dark place,Sealed in dry,Room Temperature
form :Crystalline Powder and Chunks
color :Light yellow to orange or brown
Water Solubility :Insoluble in water.
Sensitive :Air Sensitive
BRN :121302
CAS DataBase Reference :19012-03-4(CAS DataBase Reference)

Safety Information

Symbol(GHS): GHS hazard pictograms
Signal word: Warning
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H315 Causes skin irritation Skin corrosion/irritation Category 2 Warning GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 Causes serious eye irritation Serious eye damage/eye irritation Category 2A Warning GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H335 May cause respiratory irritation Specific target organ toxicity, single exposure;Respiratory tract irritation Category 3 Warning GHS hazard pictograms
Precautionary statements:
P261 Avoid breathing dust/fume/gas/mist/vapours/spray.
P264 Wash hands thoroughly after handling.
P264 Wash skin thouroughly after handling.
P271 Use only outdoors or in a well-ventilated area.
P280 Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352 IF ON SKIN: wash with plenty of soap and water.
P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

Description

1-Methylindole-3-carboxaldehyde is used as a reactant for preparation of nitroolefins and β-nitroalcohols via microwave- or ultrasound-assisted Henry reactions, reactant for synthesis of quinolinones via three-component Ugi reaction, reactant for synthesis of α-ketoamides as inhibitors of Dengue virus protease with antiviral activity in cell-culture, reactant for preparation of thiazolopyrimidinones as inhibitors of Bcl-2 proteins, reactant for preparation of vinylindoles via Peterson olefination or olefination with Nysted reagent, reactant for preparation of indolyl alkenes from microwave-enhanced Knoevenagel condensation as antibacterial agents 1-Methylindole-3-carboxaldehyde may be used in the synthesis of (Z)-3-(1-methyl-1H-indol-3-yl)-2-(thiophen-3-yl)acrylonitrile, via base-catalyzed condensation with thiophene-3-acetonitrile. It was also used in the preparation of monomer, required for the synthesis of poly(3-vinyl-1-methylindole).

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