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2-methoxynaphthalen-1-yl benzoate is a complex organic compound with the chemical formula C19H14O3. It is a derivative of naphthalene, featuring a benzoate group attached to the 1-position of the naphthalene ring, and a methoxy group at the 2-position. 2-methoxynaphthalen-1-yl benzoate is known for its potential applications in various fields, such as pharmaceuticals and materials science, due to its unique chemical structure and properties. It is characterized by its aromatic nature and the presence of both electron-donating (methoxy) and electron-withdrawing (benzoate) groups, which can influence its reactivity and interactions with other molecules. The compound is typically synthesized through chemical reactions involving naphthalene and benzoic acid derivatives, and its structure can be confirmed through spectroscopic techniques such as NMR and IR spectroscopy.

1229-49-8

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1229-49-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1229-49-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,2 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1229-49:
(6*1)+(5*2)+(4*2)+(3*9)+(2*4)+(1*9)=68
68 % 10 = 8
So 1229-49-8 is a valid CAS Registry Number.

1229-49-8Downstream Products

1229-49-8Relevant academic research and scientific papers

Visible-light-triggered direct benzoyloxylation of electron-rich arenes at room temperature without chelation assistance

Rao, Honghua,Wang, Ping,Li, Chao-Jun

supporting information, p. 6503 - 6507 (2013/01/15)

A RuII photocatalytic method was developed for the direct mono-benzoyloxylation of electron-rich aromatic and heteroaromatic systems even with an excess amount of benzoyl peroxide. The reaction was conducted at room temperature under visible light. The direct ArC-H benzoyloxylations occur without the assistance of any directing groups and can also tolerate various functional groups that have already shown diverse reactivities in transition-metal catalysis.

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