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3-(2-methoxyphenyl)furan-2,5-dione is a chemical compound with the molecular formula C10H7O4. It is a derivative of furan-2,5-dione, featuring a 2-methoxyphenyl group attached to the 3-position of the furan ring. 3-(2-methoxyphenyl)furan-2,5-dione is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is a white crystalline solid and is often used as an intermediate in organic synthesis. The compound's properties, such as its solubility and stability, can be influenced by the presence of the methoxy group, which can also affect its reactivity in various chemical reactions.

4664-99-7

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4664-99-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4664-99-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,6 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4664-99:
(6*4)+(5*6)+(4*6)+(3*4)+(2*9)+(1*9)=117
117 % 10 = 7
So 4664-99-7 is a valid CAS Registry Number.

4664-99-7Downstream Products

4664-99-7Relevant academic research and scientific papers

High-pressure-assisted addition of (methoxyphenyl)maleic anhydrides to dienes. Synthesis of 3a-aryltetrahydroisoindole-1,3-diones

Roshchin,Kuznetsov,Polunin

, p. 509 - 512 (2007)

A new synthesis of (2-and 4-methoxyphenyl)maleic anhydrides was accomplished, the reactions of which with cyclopentadiene and 3-sulfolene, serving as a 1,3-butadiene equivalent, furnished the [4+2]-cycloadducts. The latter were converted into imides of 2-

Asymmetric hydrogenation of maleic anhydrides catalyzed by Rh/bisphosphine-thiourea: efficient construction of chiral succinic anhydrides

Han, Zhengyu,Wang, Rui,Gu, Guoxian,Dong, Xiu-Qin,Zhang, Xumu

supporting information, p. 4226 - 4229 (2017/04/21)

Asymmetric hydrogenation of various 3-substituted maleic anhydrides catalyzed by Rh/bisphosphine-thiourea (ZhaoPhos) under mild conditions was successfully developed. A wide range of 3-alkyl and 3-aryl maleic anhydrides were hydrogenated well to provide the desired products 3-substituted succinic anhydrides in one hour with excellent results (full conversions, up to 99% yield, 99% ee, 3000 TON). Importantly, we developed a creative and efficient synthetic route to construct the key intermediate of the hypoglycemic drug mitiglinide through our catalytic system.

Arylmaleic anhydrides via Heck arylation of fumaric acid

Roshchin, Alexander I.

experimental part, p. 3633 - 3635 (2010/08/13)

Palladium-catalyzed arylation of fumaric acid with aryl iodides is found to be a very simple, economic and scalable approach to arylmaleic anhydrides. The reaction is facilitated by the presence of donor moieties on the aryl fragment and does not occur wi

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