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(E)-2-(2-bromovinyl)-1,4-dimethoxybenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1039359-99-3

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1039359-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1039359-99-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,9,3,5 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1039359-99:
(9*1)+(8*0)+(7*3)+(6*9)+(5*3)+(4*5)+(3*9)+(2*9)+(1*9)=173
173 % 10 = 3
So 1039359-99-3 is a valid CAS Registry Number.

1039359-99-3Relevant academic research and scientific papers

A novel method for bromodecarboxylation of α,β-unsaturated carboxylic acids using catalytic sodium nitrite

Telvekar, Vikas N.,Takale, Balaram S.

, p. 2394 - 2396 (2011)

A first novel synthetic utility of catalytic sodium nitrite in combination with aqueous HBr, for bromo decarboxylation of α,β-unsaturated carboxylic acid is described. α,β-Unsaturated carboxylic acid compounds successfully converted into corresponding bromo compounds. The advantages of this protocol are shorter reaction time and moderate to good yields.

Pd-Catalyzed Difluoromethylation of Vinyl Bromides, Triflates, Tosylates, and Nonaflates

Chang, Dalu,Gu, Yang,Shen, Qilong

supporting information, p. 6074 - 6078 (2015/04/14)

Pd-catalyzed difluoromethylation of di-, tri- or tetra-substituted vinyl bromides, triflates, tosylates and nonaflates under mild conditions is described. The reaction tolerates a wide range of functional groups, such as bromide, chloride, fluoride, ester, amine, nitrile, and protected carbonyl, thus providing a general route for the preparation of difluoromethylated alkenes. Vinyl fantasy: Pd-catalyzed difluoromethylation of di-, tri-, or tetra-substituted vinyl bromides, triflates, tosylates, and nonaflates under mild conditions is described. The reaction tolerates a wide range of functional groups, such as bromide, chloride, fluoride, ester, amine, nitrile, and protected carbonyl, thus providing a general route for the preparation of difluoromethylated alkenes.

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