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α-Chloro-β-(2,6-dichlorophenyl)propionaldehyde is a synthetic organic compound characterized by its chlorinated phenyl group and aldehyde functional group. It is a colorless to pale yellow liquid with a molecular formula of C9H6Cl3O and a molecular weight of 241.50 g/mol. α-chloro-β-(2,6-dichlorophenyl)propionaldehyde is primarily used as an intermediate in the synthesis of various agrochemicals, pharmaceuticals, and other specialty chemicals. Due to its reactive nature, it is essential to handle α-chloro-β-(2,6-dichlorophenyl)propionaldehyde with care, following proper safety protocols to minimize potential health and environmental risks.

30359-26-3

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30359-26-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30359-26-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,3,5 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 30359-26:
(7*3)+(6*0)+(5*3)+(4*5)+(3*9)+(2*2)+(1*6)=93
93 % 10 = 3
So 30359-26-3 is a valid CAS Registry Number.

30359-26-3Downstream Products

30359-26-3Relevant academic research and scientific papers

Synthesis and antitumor activities of new n-(5-benzylthiazol-2-yl)-2-(heteryl-5-ylsulfanyl)-acetamides

Ostapiuk, Yu. V.,Frolov,Vasylyschyn, R. Ya.,Matiychuk

, p. 59 - 71 (2018/05/15)

Aim. Synthesis of a series of new N-(5-benzyl-thiazol-2-yl)-2-(heteryl-5-ylsulfanyl)-acetamides and study of their anticancer activity. Methods. Organic synthesis, analytical and spectral methods, pharmacological screening. Results. [2-chloro-N-(5-aryl-1,

Process for the arylation of olefines

-

, (2008/06/13)

A process for arylating an olefinic compound by addition of an aryl group to a double bond of said olefinic compound consisting in diazotizing an arylamine in an aqueous acidic solution comprising a lower alkanoic acid to form a solution of an aryldiazonium salt and reacting said aryldiazonium salt solution with an olefinic compound in an organic solvent in the presence of a catalytically effective amount of a copper halide. The amount of alkanoic acid is about 15 to 37% by volume of the total solvents used. The alkanoic acid is preferably acetic acid and the copper halide cuprous chloride.

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