73428-03-2

Basic information

• Product Name: 3-NITRO-2-NAPHTHOIC ACID
• Synonyms: 3-NITRO-2-NAPHTHOIC ACID;3-Nitronaphthalene-2-carboxylic acid
• CAS NO: 73428-03-2
• Molecular Formula: C11H7NO4
• Molecular Weight: 217.18
• Mol File: 73428-03-2.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-NITRO-2-NAPHTHOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 3-NITRO-2-NAPHTHOIC ACID(73428-03-2)
• EPA Substance Registry System: 3-NITRO-2-NAPHTHOIC ACID(73428-03-2)

Safety Data

• Hazardous Substances Data: 73428-03-2(Hazardous Substances Data)

Usage

Uses

Used in Dye and Pigment Production:
3-Nitro-2-naphthoic acid is utilized as a key intermediate in the production of dyes, pigments, and fluorescent compounds. Its chemical properties allow for the creation of a variety of colorants used across different industries.
Used in Pharmaceutical Synthesis:
3-NITRO-2-NAPHTHOIC ACID serves as an important building block in the synthesis of pharmaceuticals. Its unique structure contributes to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Development:
3-Nitro-2-naphthoic acid is also employed in the formulation of agrochemicals, playing a role in the creation of products designed to enhance crop protection and management.
It is crucial to handle 3-Nitro-2-naphthoic acid with care due to its toxic nature if ingested or inhaled, and its potential to cause skin and eye irritation. Proper safety measures should be taken during its production, use, and disposal to minimize health and environmental risks.

Upstream product

• 77802-23-4 3-Nitro-2-naphthoesaeure-aethylester 
• 3590-37-2 ethyl 3-nitropropanoate 
• 643-79-8 o-phthalic dicarboxaldehyde 

Downstream Products

• 73428-04-3 (3-nitronaphthalen-2-yl)methanol 
• 13115-28-1 3-nitronaphthalen-2-amine 
• 77802-34-7 2-Chlormethyl-3-nitronaphthalin 

Relevant articles and documents

The Reaction of Phthalaldehydes with 3-Nitropropionates. A Simple Route to 3-Nitro-2-naphthoic Acids

3-Nitro-propionates condense with phthalaldehydes and related compounds in the presence of a base to give 3-nitro-2-naphthoic acids.

HYDROXYPHENYL NAPHTHOTRIAZOLES AS POLYMERIZABLE BLOCKERS OF HIGH ENERGY LIGHT

Described are high energy light blocking compounds and ophthalmic devices containing the compounds. In particular, described are hydroxyphenyl naphthotriazole structures with polymerizable functionality that block high energy light and are visibly transparent. The hydroxyphenyl naphthotriazole structures can be incorporated into ophthalmic devices, such as hydrogel contact lenses, to protect eyes from high energy light radiation.

NUCLEIC ACID BINDING COMPOUNDS, METHODS OF MAKING, AND USE THEREOF

The present invention relates to oligomer compounds, including dimers and trimers, formed by a disulfide, sulfinyl thio, olefin or hydrocarbon bond, or a hydrazone exchange bond between two or more monomers. Methods of making the monomers and the oligomers is also disclosed. Use of the compounds for inhibiting the activity of target RNA molecules, particularly those having a secondary structure that include a stem or stem-loop formation. Dimer compounds capable of inhibiting the activity of an HIV-1 RNA frameshifting stem-loop and a (CUG)n expanded repeat stem- loop are disclosed, as are methods of treating diseases associated with these target RNA molecules.

Arylmethyl radicals from arylmethoxybromodiazirines

(Chemical Equation Presented) Photolytic decompositions of 3-arylmethoxy-3-bromodiazirines afford arylmethyl radicals by homolyses of the diazirines' excited states.