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Home > Products >  4-Aminoindole

4-Aminoindole CAS NO.5192-23-4

  • Min.Order: 1 Gram
  • Payment Terms: T/T,MoneyGram,Other
  • Product Details

Keywords

  • 4-Aminoindole
  • 5192-23-4
  • 97% purity

Quick Details

  • ProName: 4-Aminoindole
  • CasNo: 5192-23-4
  • Molecular Formula: C8H8N2
  • Appearance: powder
  • Application: intermediate
  • DeliveryTime: in stock
  • PackAge: accroding to the need
  • Port: Shanghai Port
  • ProductionCapacity: 100 Kilogram/Day
  • Purity: 97% purity
  • Storage: Sealed in dry,Room Temperature
  • Transportation: air,sea and courier
  • LimitNum: 1 Gram
  • Grade: Industrial Grade,Pharma Grade,Electron...

Superiority

Product Name:    4-Aminoindole
Synonyms:    4-Aminoindole ,97%;4-Aminoindole;4-AMinoindole, 97% 500MG;(Indol-4-yl)amine;4-Aminoindole in stock Factory;5-methoxyl indole-carboxaldehyde;4-AMINOINDOLINE / 4-INDOLAMINE;4-AMinoindole 97%
CAS:    5192-23-4
MF:    C8H8N2
MW:    132.16
EINECS:    621-202-0
Mol File:    5192-23-4.mol                   

Details

Melting point     106-109 °C (lit.)
Boiling point     354.0±15.0 °C(Predicted)
density     1.268±0.06 g/cm3(Predicted)
storage temp.     Keep in dark place,Sealed in dry,Room Temperature
pka    18.23±0.30(Predicted)
Water Solubility     Insoluble
Sensitive     Air Sensitive
BRN     114919
CAS DataBase Reference    5192-23-4(CAS DataBase Reference)
Safety Information
Hazard Codes     Xi
Risk Statements     36/37/38
Safety Statements     26-36-24/25
WGK Germany     3
F     8-10-34
HazardClass     AIR SENSITIVE, IRRITANT-HARMFUL, KEEP COLD
HS Code     29339990
MSDS Information
Provider    Language
4-Aminoindole    English
SigmaAldrich    English
ACROS    English
ALFA    English
4-Aminoindole Usage And Synthesis
Chemical Properties    Greenish-grey to tan powder
Uses    Reactant for preparation of:• ;Inhibitors of bacterial thymidylate synthase1• ;Mimetics of non-alkaloid toxin lignan anticancer and antiviral agent Podophyllotoxin (PPT)2• ;Inhibitors of Gli1-mediated transcription in the Hedgehog pathway3• ;Protein kinase C θ (PKCθ) inhibitors4• ;Indolic non-peptidic HIV protease inhibitors5• ;Transient receptor potential cation channel subfamily V member 1 (TRPV1) antagonists6• ;Cyclooxygenase-2 (COX-2) and lipoxygenase (LOX) inhibitors7• ;11β-hydroxysteroid dehydrogenase 1 (11β-HSD1) inhibi
Synthesis Reference(s)    The Journal of Organic Chemistry, 48, p. 5130, 1983 DOI: 10.1021/jo00173a071 

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