- Indole-2-carboxylic acid
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- $0.00 / 25Kg/Drum
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2024-08-22
- CAS:1477-50-5
- Min. Order: 1KG
- Purity: 98%min
- Supply Ability: 10 ton
- Indole-2-carboxylic acid
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- $122.00 / 1KG
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2024-01-11
- CAS:1477-50-5
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: g-kg-tons, free sample is available
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| Indole-2-carboxylic acid Basic information |
| Indole-2-carboxylic acid Chemical Properties |
Melting point | 202-206 °C(lit.) | Boiling point | 287.44°C (rough estimate) | density | 1.2480 (rough estimate) | refractive index | 1.5050 (estimate) | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | solubility | Soluble in clear yellow solution 5% in ethanol, dimethyl sulfoxide and methanol. | pka | 4.44±0.30(Predicted) | form | Crystalline Powder or Crystals | color | Off-white to yellow to brown | BRN | 124132 | CAS DataBase Reference | 1477-50-5(CAS DataBase Reference) | NIST Chemistry Reference | Indole-2-carboxylic acid(1477-50-5) |
Hazard Codes | Xn,Xi | Risk Statements | 36/37/38-21/22 | Safety Statements | 22-24/25 | WGK Germany | 3 | RTECS | NK7882812 | HazardClass | IRRITANT | HS Code | 29339990 |
| Indole-2-carboxylic acid Usage And Synthesis |
Chemical Properties | Yellow Crystalline Powder | Uses | 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. | Uses | • ;Reactant for total synthesis of (±)-dibromophakellin and analogs1• ;Reactant for synthesis of the pyrrolizidine alkaloid (±)-trachelanthamidine2• ;Reactant for stereoselective preparation of renieramycin G analogs3• ;Reactant for preparation of spirooxoindolepyrrolidines via reduction of indole-2-carboxylic acid followed by oxidation, condensation, reduction, amidation and Kharasch radical cyclization4• ;Reactant for Pd-catalyzed cyclization5• ;Reactant for preparation of N,N′-(pentane)diylbis[indolecarboxamide] and N,N′-[phenylenebis( | Definition | ChEBI: Indole-2-carboxylic acid is an indolyl carboxylic acid. | Synthesis Reference(s) | Tetrahedron Letters, 33, p. 7961, 1992 DOI: 10.1016/S0040-4039(00)74789-7 |
| Indole-2-carboxylic acid Preparation Products And Raw materials |
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