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5-Methoxy-3-Methylbenzofuran is an organic compound characterized by a benzofuran ring structure, which consists of a benzene ring fused to a furan ring. This particular compound has a methyl group attached to the 3rd carbon of the benzene ring and a methoxy group (an oxygen atom bonded to a methyl group) at the 5th position. The presence of these substituents influences its chemical properties and reactivity. It is a colorless to pale yellow liquid with a molecular formula of C10H10O2 and a molecular weight of 162.19 g/mol. 5-Methoxy-3-Methylbenzofuran is primarily used as a synthetic intermediate in the preparation of various pharmaceuticals and agrochemicals, owing to its unique structure and potential biological activities.

7182-30-1

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7182-30-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7182-30-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,8 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7182-30:
(6*7)+(5*1)+(4*8)+(3*2)+(2*3)+(1*0)=91
91 % 10 = 1
So 7182-30-1 is a valid CAS Registry Number.

7182-30-1Relevant academic research and scientific papers

Silica-immobilized NHC-gold(I) complexes: Versatile catalysts for the functionalization of alkynes under batch and continuous flow conditions

Sarmiento, Jeymy T.,Suárez-Pantiga, Samuel,Olmos, Andrea,Varea, Teresa,Asensio, Gregorio

, p. 7146 - 7155 (2017/11/06)

Immobilized sterically demanding NHC-Au(I) complexes silica-[(IPrR)Au]Cl and silica-[(IAdPrR)Au]Cl are synthesized and characterized. These complexes are suitable catalysts in typical homogeneous Au(I)-catalyzed alkyne reactions such

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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