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2-Benzofurancarboxylic acid, 5-chloro-2,3-dihydro-3-hydroxy-3-methyl-, cis- is a complex organic compound with the chemical formula C10H9ClO4. It is a derivative of benzofuran, a heterocyclic aromatic compound consisting of a benzene ring fused to a furan ring. The molecule features a 5-chloro substitution on the benzofuran core, a 3-hydroxy group, and a 3-methyl group, with the cis-configuration indicating the relative positions of these substituents. 2-Benzofurancarboxylic acid, 5-chloro-2,3-dihydro-3-hydroxy-3-methyl-, cis- has potential applications in the synthesis of pharmaceuticals and agrochemicals due to its unique structure and functional groups.

142143-54-2

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142143-54-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 142143-54-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,1,4 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 142143-54:
(8*1)+(7*4)+(6*2)+(5*1)+(4*4)+(3*3)+(2*5)+(1*4)=92
92 % 10 = 2
So 142143-54-2 is a valid CAS Registry Number.

142143-54-2Downstream Products

142143-54-2Relevant academic research and scientific papers

Benzofuran Derivatives. Part 4. Synthesis of Benzofurans and 2,3,4,5-Tetrahydro-1-benzoxepin-3,5-diones

Suzuki, Tsuneo,Tanemura, Kiyoshi,Horaguchi, Takaaki,Shimimizu, Takahachi,Sakakibara, Tohru

, p. 423 - 429 (2007/10/02)

By treatment of ethyl 4- or 5-substituted 2-acetylphenoxyacetates 1 with potassium hydroxide in dry dioxane, benzofurans 2-7 and 2,3,4,5-tetrahydro-1-benzoxepin-3,5-diones 8 were obtained.The relative yields of benzofurans 2-7 and 2,3,4,5-tetrahydro-1-benzoxepin-3,5-diones 8 varied with the types of 4- or 5-substituents.The electron-donating 4-methoxyl group favored the formation of benzoxepins.On the other hand, electron-withdrawing substituents such as the 4-nitro group favored the formation of benzofurans.When esters 1 were treated with sodium amide,2,3-dihydrobenzofurans 2 were obtained exclusively regardless of 4- or 5-substituents.

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