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3-BROMO-5-NITROTOLUENE

  • Product Name 3-BROMO-5-NITROTOLUENE
  • cas 52488-28-5
  • purity 99%
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Factory Export Top Purity 3-BROMO-5-NITROTOLUENE 52488-28-5 In Stock

  • Molecular Formula: C7H6BrNO2
  • Molecular Weight: 216.034
  • Vapor Pressure: 0.012mmHg at 25°C 
  • Melting Point: 68-72 °C 
  • Refractive Index: 1.592 
  • Boiling Point: 269.5 °C at 760 mmHg 
  • Flash Point: 120 °C 
  • PSA: 45.82000 
  • Density: 1.615 g/cm3 
  • LogP: 3.18890 

3-BROMO-5-NITROTOLUENE(Cas 52488-28-5) Usage

General Description

3-Bromo-5-nitrotoluene is a chemical compound that belongs to the category of nitroaromatic compounds. It is a pale yellow solid with a molecular formula of C7H6BrNO2 and a molecular weight of 216.03 g/mol. 3-BROMO-5-NITROTOLUENE is used as a building block in the synthesis of various pharmaceuticals, dyes, and other organic compounds. It is also commonly used as an intermediate in the manufacture of agrochemicals and rubber chemicals. Additionally, 3-Bromo-5-nitrotoluene has been found to have antimicrobial activity, making it potentially useful in the development of novel antimicrobial agents. However, it is important to handle this compound with care, as it is toxic and may cause irritation to the skin, eyes, and respiratory system.

InChI:InChI=1/C7H6BrNO2/c1-5-2-6(8)4-7(3-5)9(10)11/h2-4H,1H3

52488-28-5 Relevant articles

Ipso Nitration of Aryl Boronic Acids Using Fuming Nitric Acid

Baucom, Kyle D.,Brown, Derek B.,Caille, Seb,Murray, James I.,Quasdorf, Kyle,Silva Elipe, Maria V.

supporting information, (2021/06/30)

The ipso nitration of aryl boronic acid ...

Structure-based design of highly selective 2,4,5-trisubstituted pyrimidine CDK9 inhibitors as anti-cancer agents

Shao, Hao,Foley, David W.,Huang, Shiliang,Abbas, Abdullahi Y.,Lam, Frankie,Gershkovich, Pavel,Bradshaw, Tracey D.,Pepper, Chris,Fischer, Peter M.,Wang, Shudong

supporting information, (2021/02/16)

Cyclin-dependent kinases (CDKs) are a fa...

Pd-Catalyzed Decarboxylative Ortho-Halogenation of Aryl Carboxylic Acids with Sodium Halide NaX Using Carboxyl as a Traceless Directing Group

Fu, Zhengjiang,Jiang, Yongqing,Wang, Shuiliang,Song, Yuanyuan,Guo, Shengmei,Cai, Hu

supporting information, p. 3003 - 3007 (2019/05/10)

A highly regioselective Pd-catalyzed car...

meta-Nitration of Arenes Bearing ortho/para Directing Group(s) Using C?H Borylation

Li, Xuejing,Deng, Xingwang,Coyne, Anthony G.,Srinivasan, Rajavel

supporting information, p. 8018 - 8023 (2019/05/29)

Herein, we report the meta-nitration of ...

52488-28-5 Process route

2-bromo-4-methyl-6-nitroaniline
827-24-7

2-bromo-4-methyl-6-nitroaniline

1-bromo-3-methyl-5-nitrobenzene
52488-28-5

1-bromo-3-methyl-5-nitrobenzene

Conditions
Conditions Yield
With sulfuric acid; sodium nitrite; In ethanol; at 73 - 78 ℃;
66%
2-bromo-4-methyl-6-nitroaniline; With hydrogenchloride; sodium nitrite; In water; acetic acid; at 5 - 10 ℃; for 2h;
With hypophosphorous acid; In water; acetic acid; at 0 - 20 ℃; for 48h;
64%
With ethanol; cis-nitrous acid;
With sulfuric acid; sodium nitrite; Erwaermen der erhaltenen Diazoniumsalz-Loesung mit Kupfer-Pulver;
With hypophosphorous acid; Yield given. Multistep reaction; 1) diazotization;
With sulfuric acid; sodium nitrite; In ethanol;
With copper(I) oxide; sulfuric acid; hypophosphorous acid; sodium nitrite; Yield given. Multistep reaction; 1.) H2O, -2 deg C - -3 deg C, 2 h, 2.) H2O, -5 deg C, 90 min; 0 deg C, 10 min;
With sulfuric acid; N,N-dimethyl-formamide; sodium nitrite; Yield given. Multistep reaction; 1.) water, 2.) water;
bei der Entamidierung;
Multi-step reaction with 2 steps
1: aqueous HCl / Diazotization. Kochen der Diazoniumsalz-Loesung mit KI
2: copper-powder / 230 °C
With hydrogenchloride; copper;
With sulfuric acid; sodium nitrite; In ethanol; at 73 - 78 ℃; for 0.916667h;
(3-bromo-5-methylphenyl)boronic acid
849062-36-8

(3-bromo-5-methylphenyl)boronic acid

1-bromo-3-methyl-5-nitrobenzene
52488-28-5

1-bromo-3-methyl-5-nitrobenzene

Conditions
Conditions Yield
With nitric acid; In 1,2-dichloro-ethane; at 70 ℃; for 16h; Inert atmosphere;
99%

52488-28-5 Upstream products

  • 500728-37-0
    500728-37-0

    1-bromo-2-iodo-5-methyl-3-nitrobenzene

  • 827-24-7
    827-24-7

    2-bromo-4-methyl-6-nitroaniline

  • 102170-56-9
    102170-56-9

    2-bromo-6-methyl-4-nitroaniline

  • 77811-44-0
    77811-44-0

    4-bromo-2-methyl-6-nitroaniline

52488-28-5 Downstream products

  • 124289-22-1
    124289-22-1

    5-methyl-3-nitrobenzonitrile

  • 1071718-57-4
    1071718-57-4

    N ,N '-bis-(3-bromo-5-methyl-phenyl)-hydrazine

  • 97378-75-1
    97378-75-1

    bis-(3-bromo-5-methyl-phenyl)-diazene

  • 113882-33-0
    113882-33-0

    5-Methyl-3-nitrobenzoic acid

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