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dimethyl (4R,5R)-2-phenyl-2-dodecyl-1,3-dioxolane-4,5-dicarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1411975-13-7

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1411975-13-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1411975-13-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,1,9,7 and 5 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1411975-13:
(9*1)+(8*4)+(7*1)+(6*1)+(5*9)+(4*7)+(3*5)+(2*1)+(1*3)=147
147 % 10 = 7
So 1411975-13-7 is a valid CAS Registry Number.

1411975-13-7Downstream Products

1411975-13-7Relevant academic research and scientific papers

Synthesis of new chiral and racemic 1,3-dioxolanes

Kuecuek, Hatice Baspinar,Yusufoglu, Ayse

, p. 1066 - 1070,5 (2012/12/12)

A series of chiral 1,3-dioxolanes, 3-12, with >99% ee values, have been synthesized. This is the first study of chiral ketalization reaction starting from ketones with aryl, monosubstituted aryl, and long alkyl chains (C 11-AC13). Their ee values were determined by chiral high-performance liquid chromatography (HPLC) on Chiralcel OD column, using their racemic 1,3-dioxolanes rac-3-12, which were also synthesized for the first time. These chiral and racemic 1,3-dioxolanes were characterizated by infrared, NMR (1H, 13C), mass spectrometry, elemental analysis, optical rotation, and chiral HPLC.

Synthesis of new chiral and racemic 1,3-dioxolanes

Kuecuek, Hatice Baspinar,Yusufoglu, Ayse

, p. 1066 - 1070 (2013/01/15)

A series of chiral 1,3-dioxolanes, 3-12, with >99% ee values, have been synthesized. This is the first study of chiral ketalization reaction starting from ketones with aryl, monosubstituted aryl, and long alkyl chains (C 11-AC13). Their ee values were determined by chiral high-performance liquid chromatography (HPLC) on Chiralcel OD column, using their racemic 1,3-dioxolanes rac-3-12, which were also synthesized for the first time. These chiral and racemic 1,3-dioxolanes were characterizated by infrared, NMR (1H, 13C), mass spectrometry, elemental analysis, optical rotation, and chiral HPLC.

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