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1H,3H-8-acetyl-4,5-dihydronaphto[1,2-c:4,3-b']difuran-1-one is a complex organic compound with a unique chemical structure. It is characterized by a naphthalene core, which is a fused ring system consisting of two benzene rings. The compound features a 1,2-c:4,3-b' difuran bridge, which connects the two benzene rings through furan rings. Additionally, it has an acetyl group attached to the 8-position of the naphthalene core, and the compound is in a 1H,3H-4,5-dihydro state, indicating that the molecule has undergone a reduction process, resulting in two hydrogen atoms being added to the molecule. This specific arrangement of atoms and functional groups gives the compound its distinct chemical properties and potential applications in various fields, such as pharmaceuticals or materials science.

94243-46-6

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94243-46-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94243-46-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,2,4 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 94243-46:
(7*9)+(6*4)+(5*2)+(4*4)+(3*3)+(2*4)+(1*6)=136
136 % 10 = 6
So 94243-46-6 is a valid CAS Registry Number.

94243-46-6Downstream Products

94243-46-6Relevant academic research and scientific papers

Spirocyclopropane compounds. V. One-step synthesis of 5-acetyl-spiro[benzofuran-2(3H),1'-cyclopropan]-3-one

Watanabe,Kawada,Takamoto,et al.

, p. 3373 - 3377 (2007/10/02)

5-Acetylspiro[benzofuran-2(3H),1'-cyclopropan]-3-one (3a, AG-629), previously found to be the most potent antiulcer compound in a series of spirocyclopropanes, was obtained by one step synthesis starting from methyl 5-acetyl-2-[(tetrahydro-2-oxo-3-furanyl)oxy]benzoate (1a). In this reaction, 5,10'-(diacetyl-5',6'-dihydrospiro[benzofuran-2(3H),4'(3'H)-[2H]oxocino[3, 2-b]-benzofuran]-3-one (5a), which has a new ring system, and 1H,3H-8-acetyl-4,5-dihydro-naphtho[1,2-c:4,3-b']difuran-1-one (6) were isolated as by-products. A possible reaction mechanism is presented.

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