Promotional price valid on web orders only. Your contract pricing may differ. Interested in signing up for a dedicated account number?
Learn More
  1. Home
  2. Products
  3. Chemicals
  4. Organic compounds
  5. Unclassified Organic Compounds
  6. Sigma Aldrich N-Hydroxytetrachlorophthalimide 

Sigma Aldrich N-Hydroxytetrachlorophthalimide

Catalog No. ALD0056450G Shop All MilliporeSigma Sigma Organic Chemistry Products
Encompass
Change view
Click to view available options
Quantity:
1 g
10 g
100 g
3 product options available for selection
Product selection table with 3 available options. Use arrow keys to navigate and Enter or Space to select.
Catalog No. Quantity
ALD0056450G 1 g
ALD005641G 10 g
ALD0056410G 100 g
Use arrow keys to navigate between rows. Press Enter or Space to select a product option. 3 options available.
3 options
Danger
Catalog No. ALD0056450G Supplier Sigma Aldrich Supplier No. ALD0056450G
Only null left
Add to Cart
Add to Cart
Danger

Description

MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.

N-Hydroxytetrachlorophthalimide (TCNHPI) is an aryl-tetrahalogenated N-hydroxyphthalimide derivative. In combination with 1,4-diamino-2,3-dichloroanthraquinone (DADCAQ), it forms an efficient catalytic system for the oxidation of aromatic hydrocarbons using molecular oxygen under metal-free and aerobic conditions.New reagent enabling the electrochemical allylic C-H oxidation reaction developed by the Baran group. This method provides a scalable and sustainable alternative to current strategies based on toxic reagents or precious metals.Electrochemical Allylic C–H Oxidation with N-Hydroxytetrachlorophthalimide (TCNHPI)Scalable and sustainable electrochemical allylic C–H oxidationA general alkyl-alkyl cross-coupling enabled by redox-active esters and alkylzinc reagentsNickel-Catalyzed Cross-Coupling of Redox-Active Esters with Boronic AcidsPractical Ni-Catalyzed Aryl-Alkyl Cross-Coupling of Secondary Redox-Active Esters

Specifications

CAS 85342-65-0
Molecular Formula C8HCl4NO3
Linear Formula C8HCl4NO3
Quantity 1 g
Synonym 4,5,6,7-Tetrachloro-2-hydroxy-1H-isoindole-1,3(2H)-dione; Tetrachloro-N-hydroxyphthalimide
Molecular Weight (g/mol) 300.91 g/mol
Product Title
Select an issue

By clicking Submit, you acknowledge that you may be contacted by Fisher Scientific in regards to the feedback you have provided in this form. We will not share your information for any other purposes. All contact information provided shall also be maintained in accordance with our Privacy Policy.