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2-amino-4-(2,3-dimethoxyphenyl)-4H-benzo[h]chromene-3-carbonitrile is a complex organic compound with a molecular formula of C20H16N2O3. It is characterized by a benzo[h]chromene core, which is a type of chromone with a benzene ring fused to the chromone structure. The compound features a 2-amino group, which is an amino group attached to the second carbon of the benzene ring, and a 3-carbonitrile group, indicating the presence of a nitrile group (C≡N) at the third position. Additionally, the compound has a 2,3-dimethoxyphenyl group, which is a phenyl ring with two methoxy groups (-OCH3) attached at the second and third carbons. This molecule is likely to be of interest in the field of medicinal chemistry due to its potential biological activities, such as its use as a precursor in the synthesis of various pharmaceuticals or as a compound with potential therapeutic properties.

5309-79-5

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5309-79-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5309-79-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,0 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5309-79:
(6*5)+(5*3)+(4*0)+(3*9)+(2*7)+(1*9)=95
95 % 10 = 5
So 5309-79-5 is a valid CAS Registry Number.

5309-79-5Upstream product

5309-79-5Downstream Products

5309-79-5Relevant academic research and scientific papers

Reactions of Nitrosonium Ethyl Sulfate with Olefins and Dienes: An Experimental and Theoretical Study

Zyk, Nikolai V.,Nesterov, Evgueni E.,Khlobystov, Andrei N.,Zefirov, Nikolai S.,Barnhurst, Loren A.,Kutateladze, Andrei G.

, p. 7121 - 7128 (1999)

Nitrosonium ethyl sulfate (1), which is generated in situ from ethyl nitrite and sulfur trioxide, is a convenient reagent for the one-pot transformation of olefins and dienes into substituted aldehydes and ketones. New experimental and theoretical aspects of this reaction are discussed. A DFT and ab initio computational study is undertaken to provide further insight into the mechanism of electrophilic nitrosation, including the initial π-complexes, transition states, and the intermediates involved in subsequent carbonyl formation.

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