missing translation for 'onlineSavingsMsg'
Learn More
  1. Home
  2. Products
  3. Chemicals
  4. Organic compounds
  5. Organic acids and derivatives
  6. Carboxylic acids and derivatives
  7. Monocarboxylic acids and derivatives
  8. Indole-2-carboxylic acid, 98+%

Indole-2-carboxylic acid, 98+%

Product Code. 11482968
Click to view available options
Quantity:
10 g
50 g
Unit Size:
10g
50g
This item is not returnable. View return policy

Product Code. 11482968

Brand: Thermo Scientific Alfa Aesar A18690.09

Request Bulk or Custom Format

Please to purchase this item. Need a web account? Register with us today!

This item has been discontinued and is no longer available. View the product for possible alternatives or contact our Technical Support team on 056 260 260 for assistance.
 View alternative products

This item is not returnable. View return policy

Description

CAS: 1477-50-5 | C9H7NO2 | 161.16 g/mol

Reactant for total synthesis of (±)-dibromophakellin and analogs, synthesis of the pyrrolizidine alkaloid (±)-trachelanthamidine, stereo selective preparation of renieramycin G analogs, preparation of spirooxoindolepyrrolidines via reduction of indole-2-carboxylic acid followed by oxidation, condensation, reduction, amidation and Kharasch radical cyclization, Pd-catalyzed cyclization and N,N-(pentane)diylbis[indolecarboxamide] and N,N-[phenylenebis(methylene)]bis[indolecarboxamide] derivatives.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Reactant for total synthesis of (±)-dibromophakellin and analogs, synthesis of the pyrrolizidine alkaloid (±)-trachelanthamidine, stereo selective preparation of renieramycin G analogs, preparation of spirooxoindolepyrrolidines via reduction of indole-2-carboxylic acid followed by oxidation, condensation, reduction, amidation and Kharasch radical cyclization, Pd-catalyzed cyclization and N,N′-(pentane)diylbis[indolecarboxamide] and N,N′-[phenylenebis(methylene)]bis[indolecarboxamide] derivatives.

Solubility
Soluble in clear yellow solution 5% in ethanol, dimethyl sulfoxide and methanol.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from oxidizing agent.
TRUSTED_SUSTAINABILITY

Chemical Identifiers

CAS 1477-50-5
Molecular Formula C9H7NO2
Molecular Weight (g/mol) 161.16
MDL Number MFCD00005611
InChI Key HCUARRIEZVDMPT-UHFFFAOYSA-N
Synonym indole-2-carboxylic acid, 2-carboxyindole, 2-indolecarboxylic acid, indol-2-carboxylic acid, 1h-indolecarboxylic acid, indole-2-carboxylate, 2-indolylformic acid, 2-indole carboxylic acid, 1h-indol-2-carbons, carboxyindole
PubChem CID 72899
IUPAC Name 1H-indole-2-carboxylic acid
SMILES OC(=O)C1=CC2=CC=CC=C2N1

Specifications

Melting Point ∼205°C (decomposition)
Quantity 10 g
Beilstein 124132
Solubility Information Soluble in clear yellow solution 5% in ethanol,dimethyl sulfoxide and methanol.
Formula Weight 161.16
Percent Purity ≥98%
Chemical Name or Material Indole-2-carboxylic acid

RUO – Research Use Only

Product Content Correction

Your input is important to us. Please complete this form to provide feedback related to the content on this product.

Product Title

By clicking Submit, you acknowledge that you may be contacted by Fisher Scientific in regards to the feedback you have provided in this form. We will not share your information for any other purposes. All contact information provided shall also be maintained in accordance with our Privacy Policy.

Thank You! Your feedback has been submitted. Fisher Scientific is always working to improve our content for you. We appreciate your feedback.