366633
1-(Phenylsulfonyl)indole
98%
Synonym(s):
1-(Benzenesulfonyl)indole, Benzenesulfonic acid indolide, NSC 237040, NSC 683530
Sign Into View Organizational & Contract Pricing
All Photos(2)
About This Item
Recommended Products
Assay
98%
mp
78-80 °C (lit.)
SMILES string
O=S(=O)(c1ccccc1)n2ccc3ccccc23
InChI
1S/C14H11NO2S/c16-18(17,13-7-2-1-3-8-13)15-11-10-12-6-4-5-9-14(12)15/h1-11H
InChI key
VDWLCYCWLIKWBV-UHFFFAOYSA-N
Application
1-(Phenylsulfonyl)indole may be used in the preparation of 2-acyl-1-(phenylsulfonyl)indoles. It may be used in the synthesis of starting reagent required for the synthesis of the potentially useful intermediate, 1-(phenylsulfonyl)indol-3-yl trifluoromethanesulfonate (triflate).
Reactant for preparation of:
- Antiplasmodial agents
- Antifungal agents
- Anti HIV-1 agents
- Agonists of the histamine H4 receptor
- Antibacterial agents
- Camalexin analogs
- CDK inhibitors and cytotoxic agents
- Histone Deacetylase inhibitors
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Synthesis of 1-(phenylsulfonyl) indol-3-YL trifluoromethanesulfonate.
Heterocycles, 30(1), 627-633 (1990)
A direct lithiation route to 2-acyl-1-(phenylsulfonyl) indoles.
Synthetic Communications, 32(13), 2035-2040 (2002)
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