Indole-2-carboxylic...

Indole-2-carboxylic acid
Indole-2-carboxylic acid
Indole-2-carboxylic acid

Indole-2-carboxylic acid

Min.Order / FOB Price:Get Latest Price

100 Metric Ton

Negotiable

  • Min.Order :100 Metric Ton
  • Purity: 98%min
  • Payment Terms : L/C,T/T,,MoneyGram,Other

Keywords

1477-50-5 Indole-2-carboxylic acid seller in China Sell high quality 1477-50-5 produced in China factory

Quick Details

  • Appearance:Yellow crystalline powder
  • Application:Used for research and industrial manufacture.Organic Chemistry
  • PackAge:As customer request
  • ProductionCapacity:100|Metric Ton|Day
  • Storage:Store in a cool,dry place and keep away from direct strong light
  • Transportation:Common products:Sea/Air/Courier Dangerous Chem:Sea/Air

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Details:


Preview
CBNumber: CB7728231
Chemical Name: Indole-2-carboxylic acid
Molecular Formula: C9H7NO2
Formula Weight: 161.16
CAS No.: 1477-50-5
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 Reference 1477-50-5(CAS DataBase Reference)
NIST Chemistry Reference ACROS English
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Indole-2-carboxylic acid Usage And Synthesis
Chemical Properties Yellow 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 materials 3-Indoleformic acid
Preparation Products Methyl 1H-indole-2-carboxylate-->3-Indolepropionic acid-->Indoline-2-carboxylic acid

 

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