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Benzeneacetaldehyde, a-methoxy-, oxime, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96301-75-6

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96301-75-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96301-75-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,3,0 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 96301-75:
(7*9)+(6*6)+(5*3)+(4*0)+(3*1)+(2*7)+(1*5)=136
136 % 10 = 6
So 96301-75-6 is a valid CAS Registry Number.

96301-75-6Relevant academic research and scientific papers

Synthesis of Nitriles from Aldoximes and Primary Amides Using XtalFluor-E

Keita, Massaba,Vandamme, Mathilde,Paquin, Jean-Fran?ois

, p. 3758 - 3766 (2015/11/28)

The dehydration reaction of aldoximes and amides for the synthesis of nitriles using [Et2NSF2]BF4 (XtalFluor-E) is described. Overall, the reaction proceeds rapidly (normally 1 h) at room temperature in an environmentally benign solvent (EtOAc) with only a slight excess of the dehydrating agent (1.1 equiv). A broad scope of nitriles can be prepared, including chiral nonracemic ones. In addition, in a number of cases, further purification of the nitrile after the workup was not required.

REDUCTION OF NITROALKENES WITH STANNOUS CHLORIDE IN NON-ACIDIC AND NON-AQUEOUS MEDIUM. SYNTHESIS OF α-SUBSTITUTED OXIMES

Varma, Rajender S.,Kabalka, George W.

, p. 243 - 244 (2007/10/02)

α, β-Unsaturated nitroalkenes are readily reduced by SnCl2*2H2O in alcoholic media to the α-alkoxy oxime derivatives in high yields.In the presence of ethanethiol, the corresponding α-alkylthio oximes are formed.

MODEL STUDIES FOR THE TOTAL SYNTHESIS OF THE MAYTANSINOIDS BASED ON THE INTRAMOLECULAR NITRILE OXIDE-OLEFIN CYCLOADDITION REACTION

Ko, Soo Sung,Confalone, Pat N.

, p. 3511 - 3518 (2007/10/02)

The macrocyclization of the olefinic nitrile oxide 30 to the ansa-macrolide skeleton 37, a model for a novel approach to the maytansinoids, is described.

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