103987-83-3

Basic information

• Product Name: 1-Nitronaphthalene-2-carboxylic acid
• Synonyms: 1-Nitronaphthalene-2-carboxylic acid;1-Nitro-2-Naphthoic Acid
• CAS NO: 103987-83-3
• Molecular Formula: C₁₁H₇NO₄
• Molecular Weight: 217.17758
• Mol File: 103987-83-3.mol
• Article Data: 8

Chemical Properties

• Melting Point: 246 °C
• Boiling Point: 398.3±30.0 °C(Predicted)
• Appearance: /
• Density: 1.468±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 2.40±0.30(Predicted)
• CAS DataBase Reference: 1-Nitronaphthalene-2-carboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Nitronaphthalene-2-carboxylic acid(103987-83-3)
• EPA Substance Registry System: 1-Nitronaphthalene-2-carboxylic acid(103987-83-3)

Safety Data

• Hazardous Substances Data: 103987-83-3(Hazardous Substances Data)

Usage

General Description

1-Nitronaphthalene-2-carboxylic acid is a chemical compound that belongs to the class of nitronaphthalenes, which are commonly used in the synthesis of various organic compounds. It is a derivative of naphthalene, which contains a nitro group at the 1-position and a carboxylic acid group at the 2-position. 1-Nitronaphthalene-2-carboxylic acid has potential applications in the pharmaceutical and agrochemical industries, where it can be used as a building block for the synthesis of various bioactive molecules. Additionally, 1-Nitronaphthalene-2-carboxylic acid may also have uses in the production of dyes, pigments, and other industrial products. Its precise properties and applications are likely to be further explored in the future.

InChI:InChI=1S/C11H7NO4/c13-11(14)9-6-5-7-3-1-2-4-8(7)10(9)12(15)16/h1-6H,(H,13,14)

Upstream product

• 339015-80-4 Dimethyl-[(E)-2-(1-nitro-naphthalen-2-yl)-vinyl]-amine 
• 881-03-8 1-nitro-2-methylnaphthalene 
• 176853-40-0 2-<β-trans-(N,N-dimethylamino)ethenyl>-1-nitronaphthalene 
• 99847-19-5 (1-nitro-[2]naphthyl)-pyruvic acid 
• 7697-37-2 nitric acid 
• 93-09-4 naphthalene-2-carboxylate 
• 872287-19-9 6-hydroxy-5-nitro-benzocyclohepten-7-one 

Downstream Products

• 78508-71-1 methyl 1-nitro-2-naphthoate 
• 35092-83-2 methyl 1-amino-2-naphthoate 
• 1227924-42-6 1-amino-4-bromo-2-naphthoic acid 
• 1371535-86-2 3-((1S,2S)-2-((tert-butyldimethylsilyl)oxy)cyclohexyl)-6-((6-methylpyridin-3-yl)methyl)benzo[h]quinazolin-4(3H)-one 
• 1227923-29-6 3-[(1S,2S)-2-hydroxycyclohexyl]-6-[(6-methylpyridin-3-yl)methyl]benzo[h]quinazolin-4(3H)-one 
• 1227924-49-3 3-((1S,2S)-2-hydroxycyclohexyl)-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2yl)benzo[h]quinazolin-4(3H)-one 
• 1227924-20-0 3-((1S,2S)-2-hydroxycyclohexyl)-6-((6-(methylthio)pyridin-3-yl)methyl)benzo[h]quinazolin-4(3H)-one 
• 1227924-28-8 3-((1S,2S)-2-hydroxycyclohexyl)-6-((6-methoxypyridin-3-yl)methyl)benzo[h]quinazolin-4(3H)-one 
• 1227923-94-5 6-((6-chloropyridin-3-yl)methyl)-3-((1S,2S)-2-hydroxycyclohexyl)benzo[h]quinazolin-4(3H)-one 
• 4919-43-1 1-amino-2-naphthoic acid 
• 130956-02-4 1-nitro-[2]naphthoic acid anilide 

Relevant articles and documents

-

-

M1 RECEPTOR POSITIVE ALLOSTERIC MODULATOR COMPOUNDS AND METHODS OF USE THEREOF

The present invention is directed to compounds of Formula (I): and pharmaceutically acceptable salts thereof, wherein Q, X, Y, Z, R1, R7 and n are defined herein. The compounds of Formula (I) are M1 receptor positive allosteric modul

DIHYDROBENZOQUINAZOLINONE M1 RECEPTOR POSITIVE ALLOSTERIC MODULATORS

The present invention is directed to dihydrobenzoquinazilinone compounds of formula (I) which are M1 receptor positive allosteric modulators and that are useful in the treatment of diseases in which the M1 receptor is involved, such as Alzheimer's disease