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2,4,6-Tris(trifluoromethyl)-α-methylbenzyl alcohol is a complex organic compound characterized by its unique molecular structure. It features a benzyl alcohol backbone, which is a derivative of benzyl alcohol with an additional methyl group attached to the alpha carbon. The compound is further distinguished by the presence of three trifluoromethyl groups (-CF3), each attached to different carbon atoms at the 2, 4, and 6 positions of the benzene ring. This results in a highly fluorinated and sterically hindered molecule. The compound is known for its potential applications in various chemical and pharmaceutical processes, particularly due to its unique electronic and steric properties. It is also of interest in the field of materials science for its potential use in the development of new polymers and coatings. The synthesis of such compounds often involves multi-step organic reactions and can be challenging due to the need for precise control over the introduction of the trifluoromethyl groups.

479-29-8

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479-29-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 479-29-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,7 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 479-29:
(5*4)+(4*7)+(3*9)+(2*2)+(1*9)=88
88 % 10 = 8
So 479-29-8 is a valid CAS Registry Number.

479-29-8Relevant academic research and scientific papers

The 2,4,6-tris(trifluoromethyl)phenyl group: Methyl and vinyl ketones and related chemistry

Filler, Robert,Kong, Zhengrong,Zhang, Zhaoxu,Sinha, Arun Kr.,Li, Xiaofang

, p. 71 - 75 (1996)

2,4,6-Tris(trifluoromethyl)phenyllithium (1) reacts with acetaldehyde and acrolein to give the corresponding alcohols 5 and 8. Oxidation of the alcohols with the CrO3-pyridine complex affords the acetophenone 3 and the vinyl ketone 7 respectively. The reactions of 1 with trifluoroacetic anhydride and trimethylsilyl trifluoroacetate give low to moderate yields of the trifluoroacetophenone 6.

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