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3-carboxy-4-hydroxybenzenediazonium tetrafluoroborate is a complex organic compound with the chemical formula C7H4BF4N2O4. It is derived from the benzenediazonium family, characterized by the presence of a diazonium group (-N2+) attached to a benzene ring. The molecule features a carboxylic acid group (-COOH) at the 3-position and a hydroxyl group (-OH) at the 4-position of the benzene ring. The tetrafluoroborate ion (BF4-) acts as a counterion, providing stability to the overall structure. 3-carboxy-4-hydroxybenzenediazonium tetrafluoroborate is often used as an intermediate in the synthesis of various dyes, pigments, and pharmaceuticals, and is known for its reactivity and versatility in chemical transformations.

2263-65-2

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2263-65-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2263-65-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,6 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2263-65:
(6*2)+(5*2)+(4*6)+(3*3)+(2*6)+(1*5)=72
72 % 10 = 2
So 2263-65-2 is a valid CAS Registry Number.

2263-65-2Upstream product

2263-65-2Relevant academic research and scientific papers

Synthesis of mutual azo prodrugs of anti-inflammatory agents and peptides facilitated by α-aminoisobutyric acid

Kennedy, David A.,Vembu, Nagarajan,Fronczek, Frank R.,Devocelle, Marc

, p. 9641 - 9647 (2011)

Reported is the synthesis of azo mutual prodrugs of the nonsteroidal anti-inflammatory agents (NSAIDs) 4-aminophenylacetic acid (4-APAA) or 5-aminosalicylic acid (5-ASA) with peptides, including an antibiotic peptide temporin analogue modified at the amin

Mizoroki-heck reactions with 4-phenoldiazonium salts

Schmidt, Bernd,Hoelter, Frank,Berger, Rene,Jessel, Soenke

supporting information; experimental part, p. 2463 - 2473 (2010/12/25)

Significantly better yields were achieved in Mizoroki-Heck reactions using 4-phenoldiazonium salts instead of their O-alkylated analogues under otherwise identical conditions. We found that a one-flask deacetylation-diazotation- precipitation sequence starting from paracetamol or acetanilides derived thereof provides a convenient access to the required diazonium tetrafluoroborates. The utility of these arylating agents in palladium-catalyzed C-C bond forming reactions was demonstrated for a one-flask-synthesis of the heterocyclic core of the drug aripiprazole. Notably, the diazonium salt formation from an acetanilide could be combined with two Pd-catalyzed steps in a one-flask sequence, without any exchange of solvents or isolation of intermediates.

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