1H-Indole-6-carboxy...

1H-Indole-6-carboxylic acid , 95+%

1H-Indole-6-carboxylic acid , 95+%

Min.Order / FOB Price:Get Latest Price

1 Metric Ton

Negotiable

  • Min.Order :1 Metric Ton
  • Purity: 99%
  • Payment Terms : L/C,D/A,D/P,T/T,,MoneyGram

Keywords

1670-82-2 1H-Indole-6-carboxylic acid , 95+% C9H7NO2

Quick Details

  • Appearance:yellow-beige to orange-brown powder
  • Application:Reagent
  • PackAge:as per buyers
  • ProductionCapacity:10|Metric Ton|Day
  • Storage:R.T.
  • Transportation:as per msds

Superiority:

Good quantity

Indole-6-carboxylic acid Basic information
Product Name: Indole-6-carboxylic acid
Synonyms: 6-INDOLECARBOXYLIC ACID;6-CARBOXYINDOLE;4-CARBOXAMIDOBENZOIC ACID;1H-INDOLE-6-CARBOXYLIC ACID;LABOTEST-BB LT00441293;INDOLE-6-CARBOXYLIC ACID;RARECHEM AL BE 1265;RARECHEM AL BO 0290
CAS: 1670-82-2
MF: C9H7NO2
MW: 161.16
EINECS: -0
Product Categories: blocks;Carboxes;IndolesOxindoles;Indole/indoline/oxindole;Indole and Indoline;Indoles and derivatives;Carboxylic Acids;Pyrroles & Indoles;Organic acids;Indoles;Simple Indoles;Indole;Carboxylic Acids;Pyrroles & Indoles;Building Blocks;Heterocyclic Building Blocks;Building Blocks;C7 to C9;Chemical Synthesis;Heterocyclic Building Blocks;Heterocycle-Indole series
Mol File: 1670-82-2.mol
Indole-6-carboxylic acid Structure

 

Details:

Indole-6-carboxylic acid Chemical Properties
mp  249-253 °C(lit.)
BRN  123991
CAS DataBase Reference 1670-82-2(CAS DataBase Reference)
 
Safety Information
Hazard Codes  Xn,Xi
Risk Statements  36/37/38-21/22-20/21/22-51-36-22
Safety Statements  22-24/25-37/39-26
WGK Germany  3
Hazard Note  Irritant
MSDS Information
Provider Language
SigmaAldrich English
ACROS English
ALFA English
 
Indole-6-carboxylic acid Usage And Synthesis
Chemical Properties yellow-beige to orange-brown powder
Usage • ;Reactant for preparation of D-glutamic acid-based inhibitors of E. coli MurD ligase1• ;Reactant for preparation of indolylindazoles and indolylpyrazolopyridines as interleukin-2 inducible T cell kinase inhibitors2• ;Reactant for preparation of amide conjugates with ketoprofen, as inhibitors of Gli1-mediated transcription in Hedgehog pathway3• ;Reactant for preparation of piperazine-bisamide analogs as human growth hormone secretagogue receptor antagonists for treatment of obesity4• ;Reactant for preparation of pyridinyl carboxylates via esterification with chlorohyd
Usage Reactant for preparation of D-glutamic acid-based inhibitors of E. coli MurD ligase Reactant for preparation of indolylindazoles and indolylpyrazolopyridines as interleukin-2 inducible T cell kinase inhibitors Reactant for preparation of amide conju

 

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