2417-76-7 Usage
Molecular weight
275.13 g/mol
Structure
The molecule consists of a naphthalene ring with a carboxyl group (-COOH) attached to the first position and a bromine atom attached to the second position of the naphthalene ring. A methyl group (-CH3) is esterified with the carboxyl group.
Reactivity
The compound is highly reactive due to the presence of the bromine atom and the carboxyl group, allowing it to undergo various chemical reactions such as esterification, bromination, and substitution reactions.
Uses
The compound is commonly used as an intermediate in the synthesis of various organic compounds, including drugs, pesticides, and other biologically active compounds. It is also used as a building block in the synthesis of complex organic molecules.
Importance
1-Naphthalenecarboxylic acid, 2-(bromomethyl)-, methyl ester is an important compound in the field of organic chemistry due to its versatility in undergoing various chemical reactions and its wide range of applications in the synthesis of biologically active compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 2417-76-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,1 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2417-76:
(6*2)+(5*4)+(4*1)+(3*7)+(2*7)+(1*6)=77
77 % 10 = 7
So 2417-76-7 is a valid CAS Registry Number.
2417-76-7Relevant academic research and scientific papers
Cornejo, Jaime J.,Ghodsi, Shahram,Johnson, R. Douglas,Woodling, Rick,Rickburn, Bruce
, p. 3869 - 3876 (1983)
Benzoisobenzofuran (1) is formed by base-induced 1,4-elimination of either acetal 9 or 11 and may be isolated in high yield as a cristalline solid.Cycloaddition reactions of preformed 1 have been carried out with various dienophiles.These reactions may also be accomplished by heating the acetals in the presence of dienophiles and acid catalyst, where 1 is generated as an intermediate.The cycloaddition reaction of 1 and maleic anhydride is found to be reversible at higher temperature (slow at 60 deg C).Unsymmetrical dienophiles react with 1 to give equal amounts of regioisomers, and evidence points to lack of regioselectivity under both kinetically controlled and equilibrating conditions.The acetals 9 and 11 are shown to interconvert with acid catalyst at 140 deg C, where 1 is an intermediate of greater stability than the acetals; the equilibrium K for 9 -> ( - ) 11 is approximately unity.Various acid-catalyzed cycloaddition reactions of ortho esters 8 and 10, yielding polysubstituted phenanthrene derivatives, are described.
