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3,5-Dinitrophenylethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

126369-45-7

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126369-45-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126369-45-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,3,6 and 9 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 126369-45:
(8*1)+(7*2)+(6*6)+(5*3)+(4*6)+(3*9)+(2*4)+(1*5)=137
137 % 10 = 7
So 126369-45-7 is a valid CAS Registry Number.

126369-45-7Downstream Products

126369-45-7Relevant academic research and scientific papers

Enantioselectivity, swelling and stability of 4-hydroxyprolinol containing acrylic polymer beads in the asymmetric reduction of ketones

Krane Thvedt, Thor H.,Kristensen, Tor Erik,Sundby, Eirik,Hansen, Tore,Hoff, Brd Helge

, p. 2172 - 2178 (2011)

A new 4-hydroxy-α,α-diphenyl-l-prolinol containing polymethacrylate, prepared without chromatography by a large scale adaptable synthesis, has been evaluated as a catalyst in the asymmetric reduction of 1-arylethanones. Using 1-(4-bromophenyl)ethanone as the model substance, the reduction was tested with various borane sources and solvents. The best swellings of the polymer and reactivity were observed in THF using N,N-diethylaniline borane complex as the hydride source. The selectivity in the reduction of 1-(4-bromophenyl)ethanone was found to depend on the substrate concentration and catalyst loading. Using the best conditions identified, a series of 1-arylethanones was reduced to their corresponding enantioenriched secondary alcohols. High rates and ee-values were obtained in the reduction of acetophenones containing electron withdrawing groups in the aromatic ring, whereas a moderate selectivity was the result for products containing electron donating aromatic substituents. Upon recovery of the polymer beads, it was found that vacuum drying led to extensive rupturing, while the bead structure was intact if washed with methanol and air dried at atmospheric pressure. Repeated use of the polymer catalyst gave the product alcohol with a lower 90% ee. Elemental analysis showed this to be due to the loss of the chiral prolinol unit.

Contrast media

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, (2008/06/13)

The invention provides low viscosity iodinated aryl compounds, useful as X-ray contrast agents of formula I wherein n is 0 or 1, and where n is 1 each C6R5moiety may be the same or different; X denotes a bond or a group providing a 1

Iodinated x-ray contrast media

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, (2008/06/13)

The invention provides low viscosity iodinated aryl compounds, useful as X-ray contrast agents, of formula C6R6wherein three non-adjacent R groups are iodine and the remaining R groups are non-ionic, hydrophilic moieties, said compou

Contrast media

-

, (2008/06/13)

The invention provides low viscosity iodinated aryl compounds, useful as X-ray contrast agents, of formula I STR1 (wherein n is 0 or 1, and where n is 1 each C6 R5 moeity may be the same or different; each group R is a hydrogen atom,

Contrast media

-

, (2008/06/13)

The invention provides low viscosity iodinated aryl compounds, useful as X-ray contrast agents, of formula I STR1 (wherein n is 0 or 1, and where n is 1 each C6 R5 moeity may be the same or different; each group R is a hydrogen atom,

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