ALD00564

N-Hydroxytetrachlorophthalimide

Manufacturer: Sigma Aldrich

CAS Number: 85342-65-0

Synonym(S): 4,5,6,7-Tetrachloro-2-hydroxy-1H-isoindole-1,3(2H)-dione, Tetrachloro-N-hydroxyphthalimide

Select a Size

Pack Size SKU Availability Price
1 G ALD00564-1-G In Stock ₹ 2,600.00
10 G ALD00564-10-G In Stock ₹ 7,760.00
50 G ALD00564-50-G In Stock ₹ 27,810.00

ALD00564 - 1 G

₹ 2,600.00

In Stock

Quantity

1

Base Price: ₹ 2,600.00

GST (18%): ₹ 468.00

Total Price: ₹ 3,068.00

form

powder

Quality Level

100

reaction suitability

reagent type: oxidant

SMILES string

O=C1N(O)C(C2=C(Cl)C(Cl)=C(Cl)C(Cl)=C21)=O

InChI

1S/C8HCl4NO3/c9-3-1-2(4(10)6(12)5(3)11)8(15)13(16)7(1)14/h16H

InChI key

UTRBHXSKVVPTLY-UHFFFAOYSA-N

Other Options

Image Product Name Manufacturer Price Range
50-269-5621
eMolecules​ ChemScene 4567-Tetrachloro-2-hydroxyisoindoline-13-dione 25g 582642348 CS-0041560 85342-65-0 MFCD29088000 300.900 C8HCl4NO3
eMolecules​ ₹ 26,826.48
50-186-9027
Sigma Aldrich Fine Chemicals Biosciences N-Hydroxytetrachlorophthalimide | 85342-65-0 | 50G
Sigma Aldrich Fine Chemicals Biosciences ₹ 41,295.53
50-186-9026
Sigma Aldrich Fine Chemicals Biosciences N-Hydroxytetrachlorophthalimide | 85342-65-0 | MFCD29088000 | 1g
Sigma Aldrich Fine Chemicals Biosciences ₹ 5,835.19
50-186-9025
Sigma Aldrich Fine Chemicals Biosciences N-Hydroxytetrachlorophthalimide | 85342-65-0 | | 10g
Sigma Aldrich Fine Chemicals Biosciences ₹ 9,265.29
CS-0041560
4,5,6,7-Tetrachloro-2-hydroxyisoindoline-1,3-dione
ChemScene ₹ 1,540.08 - ₹ 61,603.20
AD93100
85342-65-0 | 4,5,6,7-Tetrachloro-2-hydroxyisoindoline-1,3-dione
A2B Chem ₹ 941.16 - ₹ 43,122.24

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Description

  • General description: 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.[1]
  • Application: 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.
  • Other Notes: 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

SAFETY INFORMATION

Pictograms

GHS06

Signal Word

Danger

Hazard Statements

H301

Precautionary Statements

P301 + P330 + P331 + P310

Hazard Classifications

Acute Tox. 3 Oral

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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form:
powder

Quality Level:
100

reaction suitability:
reagent type: oxidant

SMILES string:
O=C1N(O)C(C2=C(Cl)C(Cl)=C(Cl)C(Cl)=C21)=O

InChI:
1S/C8HCl4NO3/c9-3-1-2(4(10)6(12)5(3)11)8(15)13(16)7(1)14/h16H

InChI key:
UTRBHXSKVVPTLY-UHFFFAOYSA-N

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