4-Fluoroindole CAS 387-43-9 Purity >99.0% (HPLC) Factory High Quality

Short Description:

Chemical Name: 4-Fluoroindole 

CAS: 387-43-9

Purity: >99.0% (HPLC)

Appearance: Off-White to Light Yellow Powder or Liquid

High Quality, Commercial Production

E-Mail: alvin@ruifuchem.com


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Description:

Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer and supplier of 4-Fluoroindole (CAS: 387-43-9) with high quality, commercial production. Welcomed to order.

Chemical Properties:

Chemical Name 4-Fluoroindole
Synonyms 4-Fluoro-1H-Indole
CAS Number 387-43-9
CAT Number RF-PI1595
Stock Status In Stock, Production Scale Up to Tons
Molecular Formula C8H6FN
Molecular Weight 135.14
Boiling Point 90℃/0.4 mmHg (lit.)
Solubility Soluble in Methanol
Density   1.1203
Brand Ruifu Chemical

Specifications:

Item Specifications
Appearance Off-White to Light Yellow Powder or Liquid
1 H NMR Spectrum Consistent With Structure
Purity / Analysis Method >99.0% (HPLC)
Melting Point 30.0~32.0℃
Moisture (K.F) <0.50%
Total Impurities <1.00%
Solubility in Methanol Pass
Test Standard Enterprise Standard
Usage Pharmaceutical Intermediates

Package & Storage:

Package: Bottle, Aluminium foil bag, 25kg/Cardboard Drum, or according to customer's requirement.

Storage Condition: Store in sealed containers at cool and dry place; Protect from light and moisture.

Advantages:

1

FAQ:

Application:

4-Fluoroindole (CAS: 387-43-9), Reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators; Reactant for preparation of antifungal agents; Reactant for preparation of Sodium-Dependent Glucose Co-transporter 2 (SGLT2) Inhibitors for the Management of Hyperglycemia in Diabetes; Reactant for preparation of Potent  Selective Serotonin Reuptake Inhibitors; Reactant for preparation of Inhibitors of HIV-1 attachment; Reactant for preparation of monoamine reuptake inhibitors; Reactant for preparation of histone deacetylase (HDAC) inhibitors; Reactant for preparation of inhibitors of proliferation of human breast cancer cells.

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