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Naphth[1,2-d][1,2,3]oxadiazole-5-sulphonic acid is a chemical compound with the molecular formula C10H5N3O4S. It belongs to the class of oxadiazole compounds and is a sulfonic acid derivative of naphthoxadiazole. naphth[1,2-d][1,2,3]oxadiazole-5-sulphonic acid is commonly used as a fluorescent dye and a sensitizing agent in the production of light-emitting materials and devices. The presence of the sulfonic acid group makes it water-soluble and suitable for use in aqueous environments.

84-23-1

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84-23-1 Usage

Uses

Used in Light-emitting Materials and Devices:
Naphth[1,2-d][1,2,3]oxadiazole-5-sulphonic acid is used as a fluorescent dye and sensitizing agent for the production of light-emitting materials and devices. Its water-solubility and chemical properties make it suitable for use in various applications.
Used in Optical Brighteners:
naphth[1,2-d][1,2,3]oxadiazole-5-sulphonic acid is used in the manufacturing of optical brighteners, which are additives used to enhance the appearance of materials by increasing their reflectance and brightness.
Used in Fluorescent Pigments and Dyes:
Naphth[1,2-d][1,2,3]oxadiazole-5-sulphonic acid is also used in the production of fluorescent pigments and dyes, which are utilized in various industries for coloring and enhancing the visual appeal of products.
Used in Organic Electronics:
naphth[1,2-d][1,2,3]oxadiazole-5-sulphonic acid has potential applications in the field of organic electronics, such as in the production of organic light-emitting diodes (OLEDs) and organic photovoltaic cells, due to its unique properties and characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 84-23-1 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 84-23:
(4*8)+(3*4)+(2*2)+(1*3)=51
51 % 10 = 1
So 84-23-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H6N2O4S/c13-17(14,15)9-5-8-10(11-12-16-8)7-4-2-1-3-6(7)9/h1-5H,(H,13,14,15)

84-23-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name benzo[e][1,2,3]benzoxadiazole-5-sulfonic acid

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:84-23-1 SDS

84-23-1Downstream Products

84-23-1Relevant academic research and scientific papers

Method for preparing 6-nitro-2-diazo-1-naphthol-4-sulfonic acid hydrate

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Paragraph 0014; 0032; 0037-0038; 0041; 0046-0047, (2020/06/17)

The invention discloses a method for preparing 6-nitro-2-diazo-1-naphthol-4-sulfonic acid hydrate. The method comprises the following steps: carrying out a nitrosation reaction on 2-naphthol serving as a raw material, sodium nitrite and dilute sulfuric acid in a tubular reactor to generate 1-nitroso-2-naphthol, carrying out catalytic hydrogenation on the 1-nitroso-2-naphthol and hydrogen in a Raney nickel immobilized fixed bed reactor to generate 1-amino-2-naphthol, carrying out sulfonation diazotization cyclization on 1-amino-2-naphthol and nitrosyl sulfuric acid in the tubular reactor, and nitrifying with nitric acid to obtain the final product 6-nitro-2-diazo-1-naphthol-4-sulfonic acid hydrate. According to the novel synthesis method of the 6-nitro-2-diazo-1-naphthol-4-sulfonic acid hydrate, hydrogen is used for reduction in the route, nitrosyl sulfuric acid is used for sulfonation diazotization cyclization, so the problem that a large amount of solid waste is generated in a traditional route is avoided, the atom utilization rate is high, the yield is increased, the safety coefficient is increased by using a tubular process, and the method is suitable for industrial production.

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