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CAS:1074-86-8 C9H7NO Indole-4-carboxaldehyde

CAS NO.1074-86-8

  • Min.Order: 500 Gram
  • Payment Terms: L/C,T/T,Other
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Keywords

  • CAS:1074-86-8 C9H7NO Indole-4-carboxaldehyde
  • CAS:1074-86-8 C9H7NO factory price high purity 99%
  • CAS:1074-86-8 technical grade or OLED grade

Quick Details

  • ProName: CAS:1074-86-8 C9H7NO Indole-4-carboxal...
  • CasNo: 1074-86-8
  • Molecular Formula: C9H7NO
  • Appearance: white poweder
  • Application: CAS:1074-86-8 technical grade or OLED ...
  • DeliveryTime: 5 working days after cash deposit
  • PackAge: Plastic vacuum packaging bag or bucket
  • Port: depend on clients require
  • ProductionCapacity: 1 Metric Ton/Day
  • Purity: 99%
  • Storage: under the cool and dry area
  • Transportation: by express or by sea
  • LimitNum: 500 Gram
  • Grade: Industrial Grade,Food Grade,Pharma Gra...

Superiority

Indole-4-carboxaldehyde Basic information
Product Name: Indole-4-carboxaldehyde
Synonyms: INDOLE-4-CARBALDEHYDE;INDOLE-4-CARBOXALDEHYDE;INDOLE-4-ALDEHYDE;4-FORMYLINDOLE;4-INDOLECARBALDEHYDE;4-INDOLE-CARBOXALDEHYDE;1H-INDOLE-4-CARBALDEHYDE;1H-INDOLE-4-CARBOXALDEHYDE
CAS: 1074-86-8
MF: C9H7NO
MW: 145.16
EINECS:  
Product Categories: ALDEHYDE;Aldehydes;blocks;IndolesOxindoles;Indoles and derivatives;pharmacetical;Indole;Indoles;Building Blocks;Simple Indoles;Heterocycle-Indole series
Mol File: 1074-86-8.mol
Indole-4-carboxaldehyde Structure
 
Indole-4-carboxaldehyde Chemical Properties
mp  139-143 °C(lit.)
storage temp.  Keep Cold
Sensitive  Air Sensitive
CAS DataBase Reference 1074-86-8(CAS DataBase Reference)
NIST Chemistry Reference 1H-indole-4-carboxaldehyde(1074-86-8)
 
Safety Information
Hazard Codes  Xn,Xi
Risk Statements  22-36-43
Safety Statements  26-36/37
WGK Germany  3
Hazard Note  Irritant/Keep Cold
HazardClass  IRRITANT
MSDS Information
Provider Language
SigmaAldrich English
 
Indole-4-carboxaldehyde Usage And Synthesis
Chemical Properties White to dark brown solid
Usage Usually used as reactant in Biginelli reaction,preparation of antitumor agents,intramolecular Friedel-Crafts acylation,preparation of inhibitors of cell division in E. Coli,synthesis of Hantzsch pyridine-containing Schiff bases.

 

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