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1,1,1,6,6,6-hexafluoro-2,5-bis(trifluoromethyl)hex-3-yne-2,5-diol is a complex organic compound characterized by its unique molecular structure. It consists of a hex-3-yne backbone, which is a six-carbon chain with a triple bond between the third and fourth carbon atoms. The molecule is highly fluorinated, with six fluorine atoms attached to the first, first, first, sixth, sixth, and sixth carbon atoms, respectively. Additionally, it features two trifluoromethyl groups (-CF3) attached to the second and fifth carbon atoms. 1,1,1,6,6,6-hexafluoro-2,5-bis(trifluoromethyl)hex-3-yne-2,5-diol is known for its stability and unique chemical properties, which can be attributed to the presence of fluorine atoms and the triple bond in its structure. Due to its complexity, it is typically synthesized through specialized chemical processes and has potential applications in various fields, including materials science and pharmaceuticals.

647-01-8

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647-01-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 647-01-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,4 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 647-01:
(5*6)+(4*4)+(3*7)+(2*0)+(1*1)=68
68 % 10 = 8
So 647-01-8 is a valid CAS Registry Number.

647-01-8Upstream product

647-01-8Relevant academic research and scientific papers

Preparation of an aliphatic-substituted hypervalent iodine compound, tetracoordinate 1,2-iodoxetane 1-oxide, and its application to oxidation

Kano, Naokazu,Ohashi, Masaki,Hoshiba, Kazuhisa,Kawashima, Takayuki

, p. 8173 - 8175 (2007/10/03)

A tetracoordinate 1,2-iodoxetane oxide was prepared, and it oxidized alcohols to the corresponding aldehydes and ketones in good to moderate yields under mild conditions. A tetracoordinate 1,2-iodoxetane was prepared by the fluorination of a tricoordinate 1,2-iodoxetane with xenon difluoride followed by hydrolysis. The tetracoordinate 1,2-iodoxetane oxidized alcohols and a sulfide to the corresponding aldehydes and ketones, and a sulfoxide, respectively, in good to moderate yields under mild conditions.

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