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3-BROMO-2-NITROTOLUENE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 52414-97-8 Structure
  • Basic information

    1. Product Name: 3-BROMO-2-NITROTOLUENE
    2. Synonyms: 3-BROMO-2-NITROTOLUENE 98%;3-bromo-2-nitrobenzene;3-Bromo-2-nitrotoluene,98%;1-BroMo-3-Methyl-2-nitrobenzene;6-Bromo-2-methyl-1-nitrobenzene;3-BROMO-2-NITROTOLUENE;2-Nitro-3-Bromo Toluene
    3. CAS NO:52414-97-8
    4. Molecular Formula: C7H6BrNO2
    5. Molecular Weight: 216.03
    6. EINECS: N/A
    7. Product Categories: Aromatic Hydrocarbons (substituted) & Derivatives;Nitro Compounds;Nitrogen Compounds;Organic Building Blocks
    8. Mol File: 52414-97-8.mol
  • Chemical Properties

    1. Melting Point: 25-29 °C(lit.)
    2. Boiling Point: 267℃
    3. Flash Point: >230 °F
    4. Appearance: yellow crystalline low melting mass
    5. Density: 1.612 g/mL at 25 °C(lit.)
    6. Vapor Pressure: 0.0689mmHg at 25°C
    7. Refractive Index: 1.6120 (estimate)
    8. Storage Temp.: Sealed in dry,Room Temperature
    9. Solubility: N/A
    10. CAS DataBase Reference: 3-BROMO-2-NITROTOLUENE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-BROMO-2-NITROTOLUENE(52414-97-8)
    12. EPA Substance Registry System: 3-BROMO-2-NITROTOLUENE(52414-97-8)
  • Safety Data

    1. Hazard Codes: Xn
    2. Statements: 36/37/38-20/21/22
    3. Safety Statements: 36/37/39-26-22
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 52414-97-8(Hazardous Substances Data)

52414-97-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52414-97-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,4,1 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 52414-97:
(7*5)+(6*2)+(5*4)+(4*1)+(3*4)+(2*9)+(1*7)=108
108 % 10 = 8
So 52414-97-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H6BrNO2/c1-5-3-2-4-6(8)7(5)9(10)11/h2-4H,1H3

52414-97-8 Well-known Company Product Price

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  • Aldrich

  • (545732)  3-Bromo-2-nitrotoluene  97%

  • 52414-97-8

  • 545732-5G

  • 1,533.87CNY

  • Detail
  • Aldrich

  • (545732)  3-Bromo-2-nitrotoluene  97%

  • 52414-97-8

  • 545732-25G

  • 5,403.06CNY

  • Detail

52414-97-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Bromo-2-nitrotoluene

1.2 Other means of identification

Product number -
Other names 1-Bromo-3-methyl-2-nitrobenzene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:52414-97-8 SDS

52414-97-8Relevant articles and documents

Decarboxylative Halogenation and Cyanation of Electron-Deficient Aryl Carboxylic Acids via Cu Mediator as Well as Electron-Rich Ones through Pd Catalyst under Aerobic Conditions

Fu, Zhengjiang,Li, Zhaojie,Song, Yuanyuan,Yang, Ruchun,Liu, Yanzhu,Cai, Hu

, p. 2794 - 2803 (2016/04/26)

Simple strategies for decarboxylative functionalizations of electron-deficient benzoic acids via using Cu(I) as promoter and electron-rich ones by employing Pd(II) as catalyst under aerobic conditions have been established, which lead to smooth synthesis of aryl halides (-I, Br, and Cl) through the decarboxylative functionalization of benzoic acids with readily available halogen sources CuX (X = I, Br, Cl), and easy preparation of benzonitriles from decarboxylative cyanation of aryl carboxylic acids with nontoxic and low-cost K4Fe(CN)6 under an oxygen atmosphere for the first time.

GABANERGIC MODULATORS

-

Page/Page column 68, (2010/02/10)

This invention relates to the use of compounds of benzoindazole derivatives salts and solvates thereof for the preparation of a medicament for modulating alpha2 subtype GABA A receptors. The invention further relates to novel heterocyclic compounds and pharmaceutical compositions containing said compounds. In addition the invention relates to the use of compounds of formula (I) salts and solvates thereof for the preparation of a medicament for the treatment of depression, an anxiety disorder, a psychiatric disorder, a learning or cognitive disorder, a sleep disorder, a convulsive or seizure disorder or pain.

Indazole derivatives as CRF antagonists

-

Page/Page column 18, (2010/02/07)

This invention relates to compounds which are generally CRF-1 receptor antagonists and which are represented by Formula I or Formula II: wherein R3 is optionally substituted aryl or heteroaryl, R1 and R2 are as defined in

1,3-Dihydro-3-(2-hydroxy-, 2-bromo- or 2-chloroethyl)-2H-isoindol-1-one derivatives

-

, (2008/06/13)

Derivatives of 1,3-dihydro-3-(2-hydroxyethyl) -2H-isoindol-1-one are disclosed. The derivatives are useful for treating ulcers in a mammal and for preventing or decreasing the secretion or availability of excessive amounts of gastric or hydrochloric acid in a mammal suffering from hyperchlorhydria and/or associated conditions.

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