Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

457396

Sigma-Aldrich

4-Fluoroindole

97%

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C8H6FN
CAS Number:
387-43-9
Molecular Weight:
135.14
MDL number:
MFCD00055992
UNSPSC Code:
12352100
PubChem Substance ID:
24869313
NACRES:
NA.22

Quality Level

100

Assay

97%

bp

90 °C/0.4 mmHg (lit.)

mp

30-32 °C (lit.)

SMILES string

Fc1cccc2[nH]ccc12

InChI

1S/C8H6FN/c9-7-2-1-3-8-6(7)4-5-10-8/h1-5,10H

InChI key

ZWKIJOPJWWZLDI-UHFFFAOYSA-N

Related Categories

Application

  • 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

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCW4474
MKCW2595
MKCD2494
MKBT2536V
MKBQ7500V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 2

1 of 2

5-Bromoindole 99%

Sigma-Aldrich

B68607

5-Bromoindole

Indole ≥99%

Sigma-Aldrich

I3408

Indole

(Erratum)
Journal of Medicinal Chemistry, 2442-2442 null
Synthesis of (L)-4-Fluorotryptophan.
Konas DW, et al.
Synthetic Communications, 42(1), 144-152 (2012)
Journal of the Chemical Society. Perkin Transactions 1, 1765-1765 (1994)
J L Malleron et al.
Journal of medicinal chemistry, 36(9), 1194-1202 (1993-04-30)
A series of new indole derivatives (2-28) has been prepared in the search for novel 5-HT uptake inhibitors. These compounds were obtained by the condensation of N-(chloroalkyl) naphthalenesultam derivatives with the appropriate amine in presence of a base, at reflux
A synthesis of (-)-indolactam V.
Semmelhack MF and Rhee H.
Tetrahedron Letters, 34(39), 1395-1398 (1993)
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service