51719-69-8

Basic information

• Product Name: 1-BroMo-3-broMoMethyl-5-Methyl-benzene
• Synonyms: 1-BroMo-3-broMoMethyl-5-Methyl-benzene;3-Bromo-5-methylbenzylbromide
• CAS NO: 51719-69-8
• Molecular Formula: C₈H₈Br₂
• Molecular Weight: 263.95712
• Mol File: 51719-69-8.mol
• Article Data: 20

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-BroMo-3-broMoMethyl-5-Methyl-benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-BroMo-3-broMoMethyl-5-Methyl-benzene(51719-69-8)
• EPA Substance Registry System: 1-BroMo-3-broMoMethyl-5-Methyl-benzene(51719-69-8)

Safety Data

• Hazardous Substances Data: 51719-69-8(Hazardous Substances Data)

Usage

Aromatic compound

Yes

Number of bromine atoms

Three

Benzene ring

Present

Methyl group position

5th

Main uses

a. Organic synthesis
b. Intermediate in pharmaceuticals and agrochemicals production
c. Building block in synthesis of various organic compounds
d. Reagent in chemical reactions
e. Research laboratories for chemical properties and potential applications

Applications

a. Pharmaceutical industry
b. Agrochemical industry
c. Organic compound synthesis
d. Chemical research and development

Upstream product

• 556-96-7 5-bromo-1,3-xylene 
• 94-36-0 dibenzoyl peroxide 

Downstream Products

• 871116-91-5 2-(3-bromo-5-methylphenyl)acetonitrile 
• 216755-51-0 N-(3-bromo-5-methylbenzyl)methylamine 
• 1611-92-3 3-bromo-5-methylbenzaldehyde 
• 1177558-41-6 2-[(3-bromo-5-methylphenyl)methyl]-1H-isoindole-1,3(2H)-dione 
• 1372409-19-2 C₁₉H₂₂BrN 
• 1372409-14-7 C₁₉H₂₂BrN 
• 1372409-18-1 C₁₉H₂₂BrN 
• 1372409-13-6 C₁₉H₂₂BrN 
• 51719-66-5 3-bromo-5-methylphenylacetic acid 
• 58530-13-5 3-bromo-5-methyl-benzoic acid 
• 124289-21-0 3-bromo-5-methylbenzonitrile 
• 1007578-82-6 3-bromo-5-methylbenzamide 
• 124289-24-3 α-Bromo-3-bromo-5-cyanotoluene 
• 1177558-49-4 3-bromo-5-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]benzonitrile 

Relevant articles and documents

New fluorescent tetraphenylporphyrin-based dendrimers with alkene-linked fluorenyl antennae designed for oxygen sensitization

The design of porphyrin-based dendrimers featuring conjugated fluorenyl dendrons via alkene spacers allows evaluating the importance of the role of these spacers on the optical properties of interest. In the continuation of previous studies, a second-gene

Exploration of phenylpropanoic acids as agonists of the free fatty acid receptor 4 (FFA4): Identification of an orally efficacious FFA4 agonist

The long chain free fatty acid receptor 4 (FFA4/GPR120) has recently been recognized as lipid sensor playing important roles in nutrient sensing and inflammation and thus holds potential as a therapeutic target for type 2 diabetes and metabolic syndrome. To explore the effects of stimulating this receptor in animal models of metabolic disease, we initiated work to identify agonists with appropriate pharmacokinetic properties to support progression into in vivo studies. Extensive SAR studies of a series of phenylpropanoic acids led to the identification of compound 29, a FFA4 agonist which lowers plasma glucose in two preclinical models of type 2 diabetes.

Regioisomerism in the synthesis of a chiral aminotetralin drug compound: Unraveling mechanistic details and diastereomer-specific in-depth NMR investigations

During chemical process development of a novel 2-aminotetralin derivative intended for use as an antidepressant, scrutiny of the byproduct present in the drug molecule revealed a set of regioisomers. Detailed studies showed that this impurity issue origin