6307-90-0

Basic information

• Product Name: 1,2,3-TRIMETHOXY-5-NITROBENZENE
• Synonyms: 1,2,3-TRIMETHOXY-5-NITROBENZENE;NSC43302;5-NITRO-1,2,4-TRIMETHOXYBENZENE;3,4,5-Trimethoxy-1-nitrobenzene
• CAS NO: 6307-90-0
• Molecular Formula: C₉H₁₁NO₅
• Molecular Weight: 213.19
• Mol File: 6307-90-0.mol
• Article Data: 20

Chemical Properties

• Melting Point: 96-97 °C
• Boiling Point: 341.1 °C at 760 mmHg
• Flash Point: 159.2 °C
• Appearance: /
• Density: 1.23 g/cm³
• Vapor Pressure: 0.000163mmHg at 25°C
• Refractive Index: 1.521
• CAS DataBase Reference: 1,2,3-TRIMETHOXY-5-NITROBENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,3-TRIMETHOXY-5-NITROBENZENE(6307-90-0)
• EPA Substance Registry System: 1,2,3-TRIMETHOXY-5-NITROBENZENE(6307-90-0)

Safety Data

• Hazardous Substances Data: 6307-90-0(Hazardous Substances Data)

Usage

General Description

1,2,3-Trimethoxy-5-nitrobenzene is an organic compound with the chemical formula C9H11NO6. It is a yellow crystalline solid that is commonly used in the synthesis of various pharmaceuticals and organic compounds. This chemical is primarily used as an intermediate in the production of dyes, pigments, and other organic compounds. It is also used as a reagent in organic synthesis and as a building block in the preparation of various pharmaceutical drugs. 1,2,3-Trimethoxy-5-nitrobenzene is considered to be of low toxicity, but exposure to it may cause irritation to the skin, eyes, and respiratory system. It is important to handle this compound with caution and to use appropriate protective equipment when working with it.

InChI:InChI=1/C9H11NO5/c1-13-7-4-6(10(11)12)5-8(14-2)9(7)15-3/h4-5H,1-3H3

Upstream product

• 1136-86-3 methyl (3,4,5-trimethoxyphenyl) ketone 
• 118-41-2 Eudesmic acid 
• 7697-37-2 nitric acid 
• 64-19-7 acetic acid 
• 86-81-7 3,4,5-trimethoxy-benzaldehyde 
• 55020-69-4 2,6-bis-benzenesulfonyloxy-phenol 
• 3086-62-2 3,4,5-trimethoxybenzamide 
• 634-36-6 1,2,3-trimethoxybenzene 
• 32905-09-2 2,3-dimethoxy-5-nitrophenol 
• 77-78-1 dimethyl sulfate 
• 32905-15-0 5-Nitropyrogallol-2-methylether 
• 14416-24-1 3,4,5-trihydroxy-1-nitrobenzene 
• 24313-88-0 3,4,5-Trimethoxyaniline 
• 32905-18-3 5-Nitropyrogallol-1,3-dibenzolsulfonat-2-methylaether 

Downstream Products

• 14416-24-1 3,4,5-trihydroxy-1-nitrobenzene 
• 860518-52-1 1,2,3-trimethoxy-4,5-dinitro-benzene 
• 68560-20-3 2-bromo-3,4,5-trimethoxy-1-nitro-benzene 
• 860556-74-7 2-chloro-3,4,5-trimethoxy-1-nitro-benzene 
• 108130-17-2 1,3-dichloro-4,5,6-trimethoxy-2-nitro-benzene 
• 99512-65-9 1,3-dibromo-4,5,6-trimethoxy-2-nitro-benzene 
• 24313-88-0 3,4,5-Trimethoxyaniline 
• 189564-60-1 3,5-dimethoxy-4-ethoxynitrobenzene 
• 319492-60-9 2-tert-butoxy-1,3-dimethoxy-5-nitro-benzene 
• 526221-03-4 3,4,5-tris(4'-dodecyloxybenzyloxy)-1-aminobenzene 
• 526221-02-3 3,4,5-tris(4'-dodecyloxybenzyloxy)-1-nitrobenzene 
• 25245-29-8 5-iodo-1,2,3-trimethoxybenzene 

Relevant articles and documents

Compound targeting FAK and marker thereof as well as preparation method and application thereof (by machine translation)

The invention provides a compound targeting FAK, the structure of which is shown by the following formula (I), wherein R is represented by the following formula (I). 1 - F, Cl, Br, CH3 OR-OCH3 ; R2 , R3/su

Modular synthesis of polymers containing 2,5-di(thiophenyl)-N-arylpyrrole

A modular and facile route has been developed to synthesize functionalized 2,5-di(thiophen-2-yl)-1-H-arylpyrroles from readily available starting materials. These units are compatible with various polymerization conditions and are versatile building blocks for conjugated polymers. The polymers show high thermal stability and solubility in a number of solvents. Characterization of the polymers reveals a correlation between molecular packing, controllable by polymer design, and charge carrier mobility.

Screening Libraries of Semifluorinated Arylene Bisimides to Discover and Predict Thermodynamically Controlled Helical Crystallization

Synthesis, structural, and retrostructural analysis of a library containing 16 self-assembling perylene (PBI), 1,6,7,12-tetrachloroperylene (Cl4PBI), naphthalene (NBI), and pyromellitic (PMBI) bisimides functionalized with environmentally friendly AB3 chiral racemic semifluorinated minidendrons at their imide groups via m = 0, 1, 2, and 3 methylene units is reported. These semifluorinated compounds melt at lower temperatures than homologous hydrogenated compounds, permitting screening of all their thermotropic phases via structural analysis to discover thermodynamically controlled helical crystallization from propeller-like, cogwheel, and tilted molecules as well as lamellar-like structures. Thermodynamically controlled helical crystallization was discovered for propeller-like PBI, Cl4PBI and NBI with m = 0. Unexpectedly, assemblies of twisted Cl4PBIs exhibit higher order than those of planar PBIs. PBI with m = 1, 2, and 3 form a thermodynamically controlled columnar hexagonal 2D lattice of tilted helical columns with intracolumnar order. PBI and Cl4PBI with m = 1 crystallize via a recently discovered helical cogwheel mechanism, while NBI and PMBI with m = 1 form tilted helical columns. PBI, NBI and PMBI with m = 2 generate lamellar-like structures. 3D and 2D assemblies of PBI with m = 1, 2, and 3, NBI with m = 1 and PMBI with m = 2 exhibit 3.4 ? π-π stacking. The library approach applied here and in previous work enabled the discovery of six assemblies which self-organize via thermodynamic control into 3D and 2D periodic arrays, and provides molecular principles to predict the supramolecular structure of electronically active components.