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2-(2,5-dimethyl-3-furyl)-1,1-diphenylpropan-2-ol is a complex organic compound with the molecular formula C23H24O2. It is characterized by a unique structure that includes a furyl group (a five-membered aromatic ring with one oxygen atom), two methyl groups, and a diphenylpropan-2-ol moiety. 2-(2,5-dimethyl-3-furyl)-1,1-diphenylpropan-2-ol is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its diverse chemical properties. It is also recognized for its role as an intermediate in the production of certain fragrances and flavorings. The compound's specific structure and functional groups make it a valuable building block in organic chemistry, particularly in the creation of more complex molecules with specific therapeutic or sensory properties.

95717-48-9

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95717-48-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95717-48-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,7,1 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 95717-48:
(7*9)+(6*5)+(5*7)+(4*1)+(3*7)+(2*4)+(1*8)=169
169 % 10 = 9
So 95717-48-9 is a valid CAS Registry Number.

95717-48-9Relevant academic research and scientific papers

Photoreactions of Photochromic 1-(2,5-Dimethyl-3-furyl)-1-fluoren-9-ylideneethane and Related Compounds

Heller, Harry G.,Jenkins, (Mrs) Gillian A.

, p. 2877 - 2880 (2007/10/02)

1-(2,5-Dimethyl-3-furyl)-1-fluoren-9-ylideneethane and its 3-thienyl analogue, in the crystalline state and in poly(propylene isophthalate) glass, changed from pale yellow to deep blue on irradiation at 366 nm; this change is reversed on exposure to white light.In solution, the title compound was photorearranged quantitatively into 1,3-dimethylfluoranthen-2-ylpropan-2-one on exposure to u.v. light.The photochromism and photoreactions of related compounds are described.

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