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2-Butanone, 4-hydroxy-3,3-dimethyl-4-phenyl-, also known as 4-hydroxy-3,3-dimethyl-4-phenyl-2-butanone, is an organic compound with the molecular formula C12H16O2. It is a derivative of 2-butanone, featuring a hydroxyl group (-OH) at the 4-position, and a phenyl group (C6H5) attached to the 4-position as well. The molecule also contains two methyl groups (-CH3) at the 3-position, which contribute to its structure and properties. 2-Butanone, 4-hydroxy-3,3-dimethyl-4-phenyl- is characterized by its unique chemical structure, which may have potential applications in various fields, such as pharmaceuticals, agrochemicals, or as intermediates in chemical synthesis. Due to its specific functional groups and structural features, it is essential to handle and store 2-Butanone, 4-hydroxy-3,3-dimethyl-4-phenyl- with care, following proper safety guidelines and regulations.

97234-30-5

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97234-30-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97234-30-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,2,3 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 97234-30:
(7*9)+(6*7)+(5*2)+(4*3)+(3*4)+(2*3)+(1*0)=145
145 % 10 = 5
So 97234-30-5 is a valid CAS Registry Number.

97234-30-5Downstream Products

97234-30-5Relevant academic research and scientific papers

Preparation of Enolates from α-Haloketones with n-BuLi, PhMgBr, or Et2Zn via Halogen-Metal Exchange Reaction

Aoki, Yoshitaka,Oshima, Koichiro,Utimoto, Kiitiro

, p. 463 - 464 (2007/10/03)

Metal-halogen exchange of α-iodoketones was performed upon treatment with n-BuLi, PhMgBr, Et2Zn or Me3Al in ether at 0 deg C to give the corresponding metal enolates which reacted with aldehydes to provide the aldol type products in good yields.

NiCl2(PPh3)2-Zn Promoted Deallyloxycarbonylative Directed Aldol Reaction of Allyl β-Keto Carboxylates with Aldehydes th β-Hydroxy Ketones

Nokami, Junzo,Konishi, Haruhisa,Matsuura, Hiroyuki

, p. 2023 - 2026 (2007/10/02)

Regio- and chemospecific deallyloxycarbonylative aldol reaction of allyl (or -lic) α,α-disubstituted β-keto carboxylate with aldehyde was effectively promoted by Ni(0) (NiCl2(PPh3)2-Zn), in which the allyloxycarbonyl group (-COOCH2CH=CH2) was replaced to 1-hydroxyalkyl group (-CH(OH)R, R=alkyl, vinyl, aryl) under mild reaction conditions.

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