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1,3-Dibromo-2-methyl-5-nitrobenzene is a chemical compound characterized by the molecular formula C7H6Br2NO2. It presents as a yellow crystalline solid, which is insoluble in water but readily soluble in organic solvents. 1,3-Dibromo-2-methyl-5-nitrobenzene is recognized for its role as a versatile intermediate in the synthesis of a range of organic compounds and is particularly notable for its applications in the pharmaceutical and agrochemical industries.

101581-06-0

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101581-06-0 Usage

Uses

Used in Pharmaceutical Industry:
1,3-Dibromo-2-methyl-5-nitrobenzene serves as a key intermediate in the synthesis of various pharmaceuticals. It is utilized for its ability to be chemically modified to produce a spectrum of medicinally relevant compounds, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 1,3-Dibromo-2-methyl-5-nitrobenzene is employed in the production of pesticides and other crop protection agents. Its chemical properties make it a valuable component in the creation of effective and targeted agrochemicals.
Used as a Building Block in Organic Synthesis:
Beyond its direct applications, 1,3-Dibromo-2-methyl-5-nitrobenzene is an important building block in the chemical industry, used in the synthesis of a wide array of organic compounds for various purposes. Its structural features facilitate its integration into complex organic molecules, making it a useful precursor in multiple chemical reactions.
It is crucial to handle 1,3-Dibromo-2-methyl-5-nitrobenzene with caution due to its toxic and potentially harmful properties, ensuring safety measures are in place throughout its use in research and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 101581-06-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,5,8 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 101581-06:
(8*1)+(7*0)+(6*1)+(5*5)+(4*8)+(3*1)+(2*0)+(1*6)=80
80 % 10 = 0
So 101581-06-0 is a valid CAS Registry Number.

101581-06-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-dibromo-2-methyl-5-nitrobenzene

1.2 Other means of identification

Product number -
Other names 2,6-dibromo-4-nitrotoluene

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:101581-06-0 SDS

101581-06-0Relevant academic research and scientific papers

Through space interaction between ferrocenes mediated by a thioether

Meyer, G. Joel,Hall, Gabriel B.,Smith, Elliott R.,Sakamoto, Takahiro,Lichtenberger, Dennis L.,Glass, Richard S.

, p. 125 - 132 (2015)

A series of conformationally constrained 2,6-bisferrocenylphenyl thioethers were synthesized via Suzuki-Miyaura cross coupling reactions. Structural information was obtained using X-ray crystallography and dynamic 1H NMR spectroscopic studies,

BORON-CONTAINING SMALL MOLECULES

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Paragraph 0421, (2017/09/19)

Compounds, pharmaceutical formulations, and methods of treating bacterial infections are disclosed.

Efficient synthesis of rigid ladder polymers via palladium catalyzed annulation

Liu, Sheng,Jin, Zexin,Teo, Yew Chin,Xia, Yan

supporting information, p. 17434 - 17437 (2015/02/05)

We report a new method to synthesize rigid ladder polymers using efficient palladium catalyzed annulation reactions with low catalyst loading (1 mol %). Rigid ladder polymers with benzocyclobutene backbone linkages can be synthesized from copolymerization of readily accessible aryl dibromides and norbornadiene or polymerization of AB type monomers bearing norbornene and aryl bromide or triflate moieties. High molecular weight (10-40 kDa) rigid ladder polymers can be obtained with complete monomer conversions. Diverse monomers also gave different, fixed ladder polymer conformations. The ladder polymers exhibited excellent thermal stability, high carbonization yield, and large intrinsic porosity.

Dual Pharmacophores - PDE4-Muscarinic Antagonistics

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Page/Page column 49, (2009/08/18)

The present invention is directed to novel compounds of Formula (I) and pharmaceutically acceptable salts thereof, pharmaceutical compositions and their use as dual chromaphores having inhibitory activity against PDE4 and muscarinic acetylcholine receptors (mAChRs), and thus being useful for treating respiratory diseases.

Dual Pharmacophores - PDE4-Muscarinic Antagonistics

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Page/Page column 52, (2009/08/18)

The present invention relates to novel compounds of Formula (I) and their use in the treatment of respiratory diseases, including anti-inflammatory and allergic diseases such as chronic obstructive pulmonary disease (COPD), asthma, rhinitis (e.g. allergic rhinitis), atopic dermatitis or psoriasis.

Dual Pharmacophores - PDE4-Muscarinic Antagonistics

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Page/Page column 51, (2009/08/16)

The present invention is directed to novel compounds of Formula (I), pharmaceutical compositions and their use in therapy, for example as inhibitors of phosphodiesterase type IV (PDE4) and as antagonists of muscarinic acetylcholine receptors (mAChRs), in the treatment of/and or prophylaxis of respiratory diseases, including antiinflammatory and/or allergic diseases such as chronic obstructive pulmonary disease (COPD), asthma, rhinitis (e.g. allergic rhinitis), atopic dermatitis or psoriasis.

DUAL PHARMACOPHORES - PDE4-MUSCARINIC ANTAGONISTICS

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Page/Page column 128, (2009/10/09)

The present invention is directed to novel compounds of Formula's (I) - (VI), and pharmaceutically acceptable salts thereof, pharmaceutical compositions and their use in therapy, for example as inhibitors of phosphodiesterase type IV (PDE4) and as antagonists of muscarinic acetylcholine receptors (mAChRs), in the treatment of and/or prophylaxis of respiratory diseases, including inflammatory and/or allergic diseases such as chronic obstructive pulmonary disease (COPD), asthma, rhinitis (e.g. allergic rhinitis), atopic dermatitis or psoriasis.

Poly(thiaheterohelicene): A stiff conjugated helical polymer comprised of fused benzothiophene rings

Iwasaki, Tomokazu,Kohinata, Yusaku,Nishide, Hiroyuki

, p. 755 - 758 (2007/10/03)

(Chemical Equation Presented) A novel helical aromatic polymer comprised of fused benzothiophene rings, poly(thiaheterohelicene), was synthesized via an intramolecular ring-closing reaction with a controlled helicity to one-sided bias. The synthetic helic

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