939-15-1 Usage
Description
2-Bromo-3-methylnaphthalene is a chemical compound belonging to the class of organic compounds known as bromonaphthalenes. It is characterized by its structure, which includes a bromine atom and a methyl group attached to a naphthalene base, a polycyclic aromatic hydrocarbon comprising of two fused benzene rings. 2-BROMO-3-METHYLNAPHTHALENE is known for its reactivity and versatility in a variety of chemical reactions and transformations. Due to its potential risks such as irritation to eyes and skin, and its potential harmfulness if inhaled or swallowed, handling 2-bromo-3-methylnaphthalene requires proper safety precautions.
Uses
Used in Chemical Synthesis:
2-Bromo-3-methylnaphthalene is used as an intermediate in the synthesis of various chemical products. Its reactivity and versatility make it a valuable component in the production of other compounds.
Used in Industrial Processes:
2-Bromo-3-methylnaphthalene is used as a catalyst in certain industrial processes, facilitating the production of other products. Its role in these processes is crucial for achieving the desired outcomes.
Used in Research and Development:
2-Bromo-3-methylnaphthalene is used in scientific research and development as a model compound to study the properties and reactions of bromonaphthalenes. This helps in understanding the behavior of similar compounds and their potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 939-15-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 939-15:
(5*9)+(4*3)+(3*9)+(2*1)+(1*5)=91
91 % 10 = 1
So 939-15-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H9Br/c1-8-6-9-4-2-3-5-10(9)7-11(8)12/h2-7H,1H3
939-15-1Relevant articles and documents
Synthesis of Cycloproparenes via Aromatization of 7-Oxanorbornenes with Low-Valent Titanium
Mueller, Paul,Schaller, Jean-Pierre
, p. 1608 - 1617 (2007/10/02)
1H-Cyclopropanaphthalene 3c and the 2,7-diphenyl-substituted derivative 3a have been synthesized via cycloaddition of the appropriate isobenzofurans 1a and 1b to 1-bromo-2-chlorocyclopropene and aromatization of the adducts with low-valent Ti.The same procedure afforded the 2,7-dimethyl-1H-cyclopropaisoquinoline (15), but failed for the parent azacompound.Reaction of adducts of furans to 1-bromo-2-chlorocyclopropenes with low-valent Ti produced mixtures of cyclopropabenzenes 19 and 1,6-dihalogeno-1,3,5-cycloheptatrienes 18.The latter could be converted to cyclopropabenzenes with BuLi.
