29027-13-2

Basic information

• Product Name: 2-METHYL-4,6-DINITROANISOLE
• Synonyms: 2-METHYL-4,6-DINITROANISOLE;2,4-DINITRO-6-METHYLANISOLE
• CAS NO: 29027-13-2
• Molecular Formula: C₈H₈N₂O₅
• Molecular Weight: 212.15952
• Mol File: 29027-13-2.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 369.8°Cat760mmHg
• Flash Point: 183.5°C
• Appearance: /
• Density: 1.383g/cm³
• Vapor Pressure: 2.46E-05mmHg at 25°C
• Refractive Index: 1.577
• CAS DataBase Reference: 2-METHYL-4,6-DINITROANISOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-METHYL-4,6-DINITROANISOLE(29027-13-2)
• EPA Substance Registry System: 2-METHYL-4,6-DINITROANISOLE(29027-13-2)

Safety Data

• Hazardous Substances Data: 29027-13-2(Hazardous Substances Data)

Usage

InChI:InChI=1/C8H8N2O5/c1-5-3-6(9(11)12)4-7(10(13)14)8(5)15-2/h3-4H,1-2H3

Upstream product

• 578-58-5 2-methylmethoxybenzene 
• 135-02-4 ortho-anisaldehyde 
• 90-02-8 salicylaldehyde 
• 52289-93-7 o-Methoxybenzyl bromide 
• 612-16-8 (2-methoxyphenyl)methanol 
• 13073-29-5 2-methyl-6-nitrophenol 
• 99-53-6 2-methyl-4-nitrophenol 
• 861609-18-9 6-methyl-2,3,4-trinitro-anisole 
• 75581-11-2 1-iodo-4-methoxy-3-methylbenzene 
• 7697-37-2 nitric acid 
• 77-78-1 dimethyl sulfate 
• 80-48-8 methyl p-toluene sulfonate 
• 31040-84-3 4-tert-butyl-2-methylanisole 
• 108-24-7 acetic anhydride 

Downstream Products

• 56207-35-3 acetic acid-(2-methyl-4,6-dinitro-anilide) 
• 102312-37-8 2,3,5-trinitro-benzoic acid 
• 66583-76-4 2-bromo-3,5-dinitro-toluene 
• 609-97-2 2-amino-3,5-dinitro-benzoic acid 
• 6083-69-8 2-Ethoxy-3,5-dinitro-benzoesaeure 
• 609-74-5 1-methyl-2,3,5-trinitrobenzene 
• 18905-50-5 2-chloro-1-methyl-3,5-dinitrobenzene 
• 609-99-4 3,5-dinitrosalicylic acid 
• 14139-90-3 2,N-dimethyl-4,6-dinitro-aniline 
• 14139-97-0 2-Methyl-4,6-dinitro-N-neopentyl-anilin 
• 7477-94-3 2-methyl-4,6-dinitroaniline 
• 534-52-1 6-methyl-2,4-dinitrophenol 

Relevant articles and documents

Method for synthesizing nitro (hetero) aromatic hydrocarbon

The invention discloses a method for synthesizing nitro (hetero) aromatic hydrocarbon, and belongs to the field of organic synthesis. According to the method, simple (hetero) aromatic hydrocarbon is taken as an initial raw material and is stirred and reacted in an organic solvent at 40-100 DEG C under the action of a nitration reagent, a lewis acid catalyst and protective gas, and nitro (hetero) aromatic hydrocarbon can be obtained. The method provided by the invention has the advantages of cheap and easily available raw materials, mild reaction conditions, simple preparation process, good chemical selectivity, wide substrate application range, easy amplification and the like, has great application potential, and lays a good foundation for industrial production.