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3-isopropoxy-5-(1,2,2-trifluorovinyl)benzaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1381891-53-7

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1381891-53-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1381891-53-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,1,8,9 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1381891-53:
(9*1)+(8*3)+(7*8)+(6*1)+(5*8)+(4*9)+(3*1)+(2*5)+(1*3)=187
187 % 10 = 7
So 1381891-53-7 is a valid CAS Registry Number.

1381891-53-7Downstream Products

1381891-53-7Relevant academic research and scientific papers

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

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Paragraph 0068-0071, (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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