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Home > Products >  Indole-2-carboxylic acid

Indole-2-carboxylic acid CAS NO.1477-50-5

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  • 1477-50-5
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Quick Details

  • ProName: Indole-2-carboxylic acid
  • CasNo: 1477-50-5
  • Molecular Formula: C9H7NO2
  • Appearance: Yellow crystalline powder
  • Application: Used for research and industrial manuf...
  • DeliveryTime: Within 3-7 days after receipt of your ...
  • PackAge: As customer request
  • Port: Qingdao,China
  • ProductionCapacity: 100 Metric Ton/Day
  • Purity: 98%min
  • Storage: Store in a cool,dry place and keep awa...
  • Transportation: Common products:Sea/Air/Courier Dange...
  • LimitNum: 100 Metric Ton

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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
ALFA English
 
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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