Indole-2-carboxylic acid

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Products Intro: Product Name:Indole-2-carboxylic acid
CAS:1477-50-5
Purity:98% Package:10G,250G,50G
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Products Intro: Product Name:Indole-2-carboxylic acid
CAS:1477-50-5
Purity:98% Package:50g Remarks:A23001
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Products Intro: Product Name:Indole-2-carboxylic acid
CAS:1477-50-5
Purity:99% HPLC Package:1Mg ; 5Mg;10Mg ;100Mg;250Mg ;500Mg ;1g;2.5g ;5g ;10g
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Products Intro: Product Name:Indole-2-carboxylic acid, 98+%
CAS:1477-50-5
Package:10g Remarks:A18690
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Products Intro: Product Name:Indole-2-carboxylic Acid
CAS:1477-50-5
Purity:98.0%(GC&T) Package:25G;5G
Indole-2-carboxylic acid Basic information
Product Name:Indole-2-carboxylic acid
Synonyms:AKOS JY2082713;2-CARBOXYINDOLE;2-INDOLECARBOXYLIC ACID;1H-INDOLE-2-CARBOXYLIC ACID;INDOLE-1H-2-CARBOXYLIC ACID;INDOLE-2-CARBOXYLIC ACID;OTAVA-BB BB7013890553;TIMTEC-BB SBB003953
CAS:1477-50-5
MF:C9H7NO2
MW:161.16
EINECS:216-030-4
Product Categories:Indole/indoline/oxindole;indole derivative;Indole and Indoline;Indoles and derivatives;Carboxylic Acids;Pyrroles & Indoles;Indole;Organic acids;Amino Acids 13C, 2H, 15N;Indoles;Simple Indoles;Amino Acids & Derivatives;Indole Derivatives;Carboxylic Acids;Pyrroles & Indoles;Bioactive Small Molecules;Building Blocks;C7 to C9;Cell Biology;Chemical Synthesis;Heterocyclic Building Blocks;I;Heterocycle-Indole series
Mol File:1477-50-5.mol
Indole-2-carboxylic acid Structure
Indole-2-carboxylic acid Chemical Properties
mp 202-206 °C(lit.)
BRN 124132
CAS DataBase Reference1477-50-5(CAS DataBase Reference)
NIST Chemistry ReferenceIndole-2-carboxylic acid(1477-50-5)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 36/37/38-21/22
Safety Statements 22-24/25
WGK Germany 3
RTECS NK7882812
Hazard Note Irritant
HazardClass IRRITANT
HS Code 29339990
MSDS Information
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Indole-2-carboxylic acid English
SigmaAldrich English
ACROS English
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Indole-2-carboxylic acid Usage And Synthesis
Chemical PropertiesYellow Crystalline Powder
Usage• ;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(
Indole-2-carboxylic acid Preparation Products And Raw materials
Raw materials3-Indoleformic acid
Preparation ProductsMethyl 1H-indole-2-carboxylate-->3-Indolepropionic acid-->Indoline-2-carboxylic acid
Tag:Indole-2-carboxylic acid(1477-50-5) Related Product Information
2-(Ethoxycarbonyl)-5-bromo-indole 5-Hydroxyindole-2-carboxylic acid Ethyl indole-2-carboxylate ETHYL 5-NITRO-3-PHENYLINDOLE-2-CARBOXYLATE Ethyl 5-chloro-2-indolecarboxylate Ethyl 5-hydroxyindole-2-carboxylate ETHYL 5,6-DIMETHOXYINDOLE-2-CARBOXYLATE 4-BENZYLOXYINDOLE-2-CARBOXYLIC ACID ETHYL ESTER ETHYL 5-METHYLINDOLE-2-CARBOXYLATE 5-METHOXYINDOLE-2-CARBOXYLIC ACID 5-Chloroindole-2-carboxylic acid 5,6-DIMETHOXYINDOLE-2-CARBOXYLIC ACID 7-Nitroindole-2-carboxylic acid 3-HYDROXYINDOLE-2-CARBOXYLIC ACID METHYL ESTER ETHYL 5-BENZYLOXYINDOLE-2-CARBOXYLATE 5-Fluoroindole-2-carboxylic acid 1-Methylindole-2-carboxylic acid 2-CARBETHOXY-5-ETHYLINDOLE