2,6-Dibromo-3-methyl-4-nitroanisole

Base Information

• Chemical Name: 2,6-Dibromo-3-methyl-4-nitroanisole
• CAS No.: 62265-99-0
• Molecular Formula: C8H7Br2NO3
• Molecular Weight: 324.95408
• European Community (EC) Number: 263-479-7
• UNII: QB2GYZ4TV8
• DSSTox Substance ID: DTXSID9069554
• Nikkaji Number: J307.015H
• Wikidata: Q72464501
• Mol file: 62265-99-0.mol

Synonyms:62265-99-0;1,3-dibromo-2-methoxy-4-methyl-5-nitrobenzene;2,6-Dibromo-3-methyl-4-nitroanisole;Benzene, 1,3-dibromo-2-methoxy-4-methyl-5-nitro-;EINECS 263-479-7;6-Nitro-2,4-dibromo-3-methoxytoluene;1,3-Dibromo-2-methoxy-5-nitro-6-methylbenzene;Benzene,1,3-dibromo-2-methoxy-4-methyl-5-nitro-;QB2GYZ4TV8;1,3-Dibromo-2-methoxy-4-methyl-5-nitro-benzene;SCHEMBL700219;DTXSID9069554;AMY34550;MFCD23099204;AKOS027328092;2,4-Dibromo-3-methoxy-6-nitrotoluene;PB48586;AS-52525;CS-0052743;FT-0629037;P15291;1,3?dibromo?2?methoxy?4?methyl?5?nitrobenzene;1,3(c)\dibromo(c)\2(c)\methoxy(c)\4(c)\methyl(c)\5(c)\nitrobenzene

Chemical Property of 2,6-Dibromo-3-methyl-4-nitroanisole

Chemical Property:

• Vapor Pressure: 6.8E-05mmHg at 25°C
• Refractive Index: 1.602
• Boiling Point: 354.5 °C at 760 mmHg
• Flash Point: 168.2 °C
• PSA: 55.05000
• Density: 1.868 g/cm³
• LogP: 3.96000
• XLogP3: 3.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 324.87722
• Heavy Atom Count: 14
• Complexity: 221

Purity/Quality:

99% ^*data from raw suppliers

1,3-Dibromo-2-methoxy-4-methyl-5-nitrobenzene 97% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=C(C(=C(C=C1[N+](=O)[O-])Br)OC)Br
• Use Description: 2,6-dibromo-3-methyl-4-nitroanisole is a chemical compound with potential applications in various fields. In the pharmaceutical industry, it may serve as a starting material or intermediate in the synthesis of pharmaceutical compounds, potentially contributing to drug development and manufacturing processes. Its unique chemical structure suggests it may be involved in the creation of drug candidates with specific pharmacological properties. Additionally, in the field of organic chemistry, it can be used as a building block for the synthesis of complex organic molecules, aiding researchers in the development of new materials, catalysts, and specialty chemicals. While specific uses may vary depending on research and development needs, its primary significance likely lies in drug discovery and organic synthesis, making it a valuable tool for pharmaceutical researchers and chemists.