23295-00-3

Basic information

• Product Name: phenyl 6-diazo-5,6-dihydro-5-oxonaphthalene-1-sulphonate
• Synonyms: phenyl 6-diazo-5,6-dihydro-5-oxonaphthalene-1-sulphonate;5-Oxo-6-diazo-1-naphthalenesulfonic acid phenyl ester;5-Oxo-6-diazo-5,6-dihydro-1-naphthalenesulfonic acid phenyl ester;5-Oxo-6-diazo-5,6-dihydronaphthalene-1-sulfonic acid phenyl ester;6-Diazo-5,6-dihydro-5-oxo-1-naphthalenesulfonic acid phenyl ester;6-Diazo-5-oxo-1-naphthalenesulfonic acid phenyl ester;1-Naphthalenesulfonic acid, 6-diazo-5,6-dihydro-5-oxo-, phenyl ester;2-Diazo 1-naphthol 5-sulfonate ester of phenol
• CAS NO: 23295-00-3
• Molecular Formula: C₁₆H₁₀N₂O₄S
• Molecular Weight: 326.3266
• EINECS: 245-564-0
• Mol File: 23295-00-3.mol
• Article Data: 6

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: g/cm³
• CAS DataBase Reference: phenyl 6-diazo-5,6-dihydro-5-oxonaphthalene-1-sulphonate(CAS DataBase Reference)
• NIST Chemistry Reference: phenyl 6-diazo-5,6-dihydro-5-oxonaphthalene-1-sulphonate(23295-00-3)
• EPA Substance Registry System: phenyl 6-diazo-5,6-dihydro-5-oxonaphthalene-1-sulphonate(23295-00-3)

Safety Data

• Hazardous Substances Data: 23295-00-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C16H10N2O4S/c17-18-14-10-9-12-13(16(14)19)7-4-8-15(12)23(20,21)22-11-5-2-1-3-6-11/h1-10H

Upstream product

• 1001756-09-7 2-diazo-1-oxo-1,2-dihydronaphthalene-4-sulfonyl chloride 
• 108-95-2 phenol 

Downstream Products

• 117714-42-8 1-Oxomethylene-1H-indene-4-sulfonic acid phenyl ester 
• 117714-41-7 4-Phenoxysulfonyl-3H-indene-1-carboxylic acid 
• 137833-35-3 4-Phenoxysulfonyl-3H-indene-1-carboxylic acid p-tolyl ester 

Relevant articles and documents

Single Pot Process For The Preparation Of Diazonaphthoquinonesulfonyl Ester

The present invention provides a single pot process for the preparation of diazonaphthoquinonesulfonyl ester, a useful organic material for micro electronic and dye industry. This study pertains to the one pot preparation of diazonaphthoquinonesulfonyl esters using the corresponding diazonaphthoquinine sulfonic acid or its sodium salt, diphosgene or triphosgene, variety of hydroxy compounds and tertiary organic base in an organic solvent medium.

Synthesis and Characterization of Substituted 2-Diazo-1-oxo-1,2-dihydronaphthalenes and Their Products of Photolysis and Thermolysis

Several 2-diazo-1-oxo-1,2-dihydronaphthalenes (1, 2) have been synthesized by reaction of selected hydroxy compounds and 2-diazo-1-oxo-1,2-dihydronaphthalene-5- and -4-sulfonylchloride, respectively.Photolysis as well as thermolysis of 1 and 2 leads to final products, the nature of which depends on the position of substitution.So, reactions of 5-substituted derivatives (1) yield the corresponding indene-3-carboxylic acids 3 and their esters 5, respectively.In contrast, reactions of 4-substituted derivatives (2) lead to the formation of the 1-sulfo-indene-3-carboxylic acid derivatives 4 and 6.Prepared compounds have been characterized by means of mass, ultraviolet, infrared, 1H-n.m.r. and 13C-n.m.r. spectroscopy.

UV/VIS-Spectroscopical Investigations on 2-Diazo-1-oxo-1,2-dihydronaphthalen-5-sulfonic Acid Esters

-