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Trimethyl(4-(1,2,2-trifluorovinyl)phenyl)silane is an organosilicon compound characterized by its molecular formula C11H13F3Si. It features a trifluorovinyl group (CF=CF2) attached to a phenyl ring, which is further substituted with a trimethylsilyl group (SiMe3). trimethyl(4-(1,2,2-trifluorovinyl)phenyl)silane is of interest in the field of organic chemistry, particularly in the synthesis of fluorinated compounds and as a potential intermediate in the preparation of various pharmaceuticals and specialty chemicals. Its unique structure, with the combination of fluorine atoms and silicon, may confer specific reactivity and stability properties that are valuable in chemical research and industrial applications.

2972-91-0

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2972-91-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2972-91-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,7 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2972-91:
(6*2)+(5*9)+(4*7)+(3*2)+(2*9)+(1*1)=110
110 % 10 = 0
So 2972-91-0 is a valid CAS Registry Number.

2972-91-0Downstream Products

2972-91-0Relevant articles and documents

The method of manufacturing the same and hydroxybenzenes (trifluorolactic vinyl)

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Paragraph 0083-0085, (2018/10/03)

PROBLEM TO BE SOLVED: To provide (trifluorovinyl)benzenes and a method for producing the same.SOLUTION: The method for producing (trifluorovinyl)benzenes expressed by general formula (3) comprises carrying out a reaction of a phenyl boron compound with trifluorohaloethylenes in the coexistence of 1 to 100 equivalents of water with respect to the phenyl boron compound (1), a palladium complex coordinated with a bidentate phosphine ligand, and an alkali metal salt. In formula (3), Rrepresents a hydrogen atom or a formyl group; Rand Reach independently represents a hydrogen atom, 1-4C alkyl group, 2-4C alkenyl group, 2-5C acyl group, (1-4C alkoxy)carbonyl group, 1-4C alkoxy group, tri(1-4C alkyl)silyl group, 2-5C acylamino group, cyano group, phenyl group, chlorine atom, fluorine atom or nitro group; and adjoining Rand Rmay form a ring together with a carbon atom bonded thereto.

Pd-catalyzed arylation of chlorotrifluoroethylene using arylboronic acids

Yamamoto, Tetsuya,Yamakawa, Tetsu

supporting information; experimental part, p. 3454 - 3457 (2012/08/29)

The palladium-catalyzed cross-coupling of chlorotrifluoroethylene and arylboronic acids proceeds in the presence of a base and H2O to provide α,β,β-trifluorostyrene derivatives in satisfactory yields.

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