69048-70-0

Basic information

• Product Name: dimethyl 4-nitroisophthalate
• Synonyms: dimethyl 4-nitroisophthalate
• CAS NO: 69048-70-0
• Molecular Formula: C₁₀H₉NO₆
• Molecular Weight: 239.18156
• Mol File: 69048-70-0.mol
• Article Data: 13

Chemical Properties

• Melting Point: 77-80 °C
• Boiling Point: 360.2±27.0 °C(Predicted)
• Appearance: /
• Density: 1.350±0.06 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: dimethyl 4-nitroisophthalate(CAS DataBase Reference)
• NIST Chemistry Reference: dimethyl 4-nitroisophthalate(69048-70-0)
• EPA Substance Registry System: dimethyl 4-nitroisophthalate(69048-70-0)

Safety Data

• Hazardous Substances Data: 69048-70-0(Hazardous Substances Data)

Usage

Description

Dimethyl 4-nitroisophthalate is a chemical compound with the molecular formula C10H9NO6. It is a derivative of isophthalic acid, characterized by the presence of two methyl groups and a nitro group attached to the aromatic ring. This solid substance exhibits stability under normal conditions and is utilized in various organic synthesis applications.

Uses

Used in Pharmaceutical Industry:
Dimethyl 4-nitroisophthalate serves as a key building block in the synthesis of pharmaceuticals. Its unique structure allows for the development of a range of medicinal compounds, contributing to the advancement of healthcare and therapeutic options.
Used in Polymer Industry:
In the polymer industry, dimethyl 4-nitroisophthalate is employed as a crucial component in the production of specific types of polymers. Its integration into polymer formulations can enhance properties such as strength, flexibility, and durability, catering to diverse applications.
Used in Dye Industry:
Dimethyl 4-nitroisophthalate is utilized in the dye industry for the preparation of various dyes. Its chemical properties enable the creation of dyes with distinct color characteristics and improved performance, meeting the demands of different industries.
Used in Liquid Crystal Display (LCD) Industry:
dimethyl 4-nitroisophthalate also plays a significant role in the production of liquid crystal display materials. Its incorporation into LCD technologies can enhance the display's visual quality and contribute to the development of advanced electronic devices.
Safety Note:
Dimethyl 4-nitroisophthalate should be handled and stored according to standard chemical safety procedures to ensure the safety of individuals and the environment.

Upstream product

• 67-56-1 methanol 
• 4315-09-7 4-nitroisophthalic acid 
• 74-88-4 methyl iodide 
• 89-87-2 2,4-dimethylnitrobenzene 
• 3113-72-2 5-methyl-2-nitrobenzoic acid 

Downstream Products

• 63746-12-3 dimethyl 4-aminoisophthalate 
• 64152-09-6 3-Methoxycarbonyl-4-nitrobenzoic acid 
• 67667-50-9 Dimethyl-4-phenylthioisophthalat 
• 67666-73-3 4-Benzylsulfanyl-isophthalic acid dimethyl ester 
• 53063-31-3 4-phenoxy-1,3-benzenedicarboxylic acid dimethyl ester 
• 41684-07-5 4-amino-3-(methoxycarbonyl)benzoic acid 
• 67666-84-6 2,4-bis-(hydroxymethyl)diphenyl ether 
• 67666-83-5 2,4-bis-(hydroxymethyl)diphenyl sulfide 
• 67666-86-8 2,4-Bis(chloromethyl)diphenylsulfid 
• 67666-87-9 2,4-Bis-chloromethyl-1-phenoxy-benzene 
• 67666-90-4 2,4-bis-(carboxymethyl)diphenyl ether 
• 67666-89-1 2,4-bis-(carboxymethyl)diphenylsulfide 

Relevant articles and documents

SELF-IMMOLATIVE SYSTEMS

The present invention is concerned with self-immolative recognition and/or responsive systems for electrophilic compounds, especially alkylating agents, which systems may comprise disclosure or detection of the alkylating agent. The present invention is especially concerned with non-protic triggered self-immolative systems, molecules, and methods, and in particular for detection of non- protic electrophilic agents, and especially alkylating agents, for example alkyl or benzylic halides, which may be found in pesticides or fumigants, or chemical warfare agents.

Quinazolin-2,4-dione derivative and preparation method and application thereof

The invention provides a quinazolin-2,4-dione derivative and a preparation method and application thereof, and specifically, the invention provides a quinazolin-2,4-dione derivative shown as formula (I) and a composition comprising same. The invention further provides the method for preparing the derivative and the application of the derivative in selectively controlling unexpected plants among useful crops, wherein Q, W, Z, Y, R, R and R have the meanings as described by the invention. The formula (I) is as shown in the description below.

TRIKETONE COMPOUND AND PREPARATION METHOD AND USE THEREOF

Disclosed in the present invention is a triketone compound which has a structure shown in Formula (I). Also disclosed in the present invention is a method for preparing the triketone compound having a structure as shown by Formula (I), which comprise that under the rearrangement reaction conditions, the compound having a structure as shown by Formula (II) is contacted with a catalyst in the presence of a base and a solvent. Further disclosed in the present invention is the use of a triketone compound having a structure as shown by Formula (I) in preventing and controlling weeds. Said triketone compound having a structure as shown by formula (I) in the present invention has the effect of preventing and controlling weeds, in particular having an excellent effect on preventing and controlling broadleaved weeds and/or gramineae weeds.