| Identification | More | [Name]
Indole-2-carboxylic acid | [CAS]
1477-50-5 | [Synonyms]
1H-INDOLE-2-CARBOXYLIC ACID
2-CARBOXYINDOLE
2-INDOLECARBOXYLIC ACID
AKOS JY2082713
INDOLE-1H-2-CARBOXYLIC ACID
INDOLE-2-CARBOXYLIC ACID
OTAVA-BB BB7013890553
TIMTEC-BB SBB003953
indole-2-carboxlicacid
Indole-2-carboxylate acid
Indole-3-CarboxylicAcidForBiochemistry
2-IndolecarboxylicAcid:Indole-2-CarboxylicAcid
Indole-2-carboxylic acid, 98+%
2-Indolylformic Acid
NSC 16598
Indole-2-carboxylic
Indole-2-earboxylic acid ethylester | [EINECS(EC#)]
216-030-4 | [Molecular Formula]
C9H7NO2 | [MDL Number]
MFCD00005611 | [Molecular Weight]
161.16 | [MOL File]
1477-50-5.mol |
| Chemical Properties | Back Directory | [Appearance]
Yellow Crystalline Powder | [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. | [form ]
Crystalline Powder or Crystals | [pka]
4.44±0.30(Predicted) | [color ]
Off-white to yellow to brown | [Detection Methods]
HPLC | [BRN ]
124132 | [CAS DataBase Reference]
1477-50-5(CAS DataBase Reference) | [NIST Chemistry Reference]
Indole-2-carboxylic acid(1477-50-5) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn,Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin .
R21/22:Harmful in contact with skin and if swallowed . | [Safety Statements ]
S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [RTECS ]
NK7882812 | [Hazard Note ]
Irritant | [HazardClass ]
IRRITANT | [HS Code ]
29339990 |
| Hazard Information | Back Directory | [Chemical Properties]
Yellow Crystalline Powder | [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 | [IC 50]
NMDA Receptor; Human Endogenous Metabolite |
|
|