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2,2-dimethyl-1-(4-nitrophenyl)-1,3-propanediol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56010-54-9

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56010-54-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56010-54-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,0,1 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 56010-54:
(7*5)+(6*6)+(5*0)+(4*1)+(3*0)+(2*5)+(1*4)=89
89 % 10 = 9
So 56010-54-9 is a valid CAS Registry Number.

56010-54-9Relevant academic research and scientific papers

Optical enrichment in enzyme-catalyzed resolution of 1-aryl-2,2-dimethyl-1,3-propanediols

Mukherjee, Chandrani,Mohapatra, Prabhu P.,Youssef, Dani,Jha, Amitabh

, p. 1 - 6 (2017/01/10)

Novozym 435 efficiently catalyzed the chemo-, regio-, and enantioselective transesterification of 1-aryl-2,2-dimethyl-1,3-propanediols in different organic solvents with vinyl acetate as the acetyl donor at room temperature. This enzyme-catalyzed chemical

Biheteroaromatic diphosphine oxides-catalyzed stereoselective direct aldol reactions

Rossi, Sergio,Benaglia, Maurizio,Genoni, Andrea,Benincori, Tiziana,Celentano, Giuseppe

supporting information; experimental part, p. 158 - 166 (2011/02/27)

A highly stereoselective direct aldol condensation of ketones to aromatic aldehydes was realized; the trichlorosilyl enolether generated in situ in the presence of tetrachlorosilane is activated by catalytic amounts of an enantiomerically pure biheteroaromatic phosphine oxide to react with aldehydes, coordinated as well as activated by the chiral cationic hypervalent silicon species. This Lewis acid-mediated Lewis base-catalyzed transformation allowed, starting from two carbonyl compounds, to directly synthesize β-hydroxy ketones generally with high anti stereoselectivity and up to 93% ee for the anti isomer.

Asymmetric cyclic phosphorothonamides containing substituted pyridine

Shi, De-Qing,Feras, Abudhaim,Liu, Yi

, p. 2663 - 2673 (2007/10/03)

In order to find high-acitivity and low-toxicity pesticidal lead compounds, a type of novel, asymmetric cyclic phosphorothonamides containing substituted pyridine were synthesized via the condensation reactions of 2-chloro-4- substitutedphenyl-5,5-dimethy

Lithium acetate-catalyzed crossed aldol reaction between aldehydes and trimethylsilyl enolates generated from other aldehydes

Kawano, Yoshikazu,Fujisawa, Hidehiko,Mukaiyama, Teruaki

, p. 614 - 615 (2007/10/03)

Crossed aldol reaction between aromatic aldehydes having an electron-withdrawing group and trimethylsilyl enolates generated from several aldehydes proceeded smoothly in dry or water-containing DMF in the presence of a catalytic amount of a Lewis base such as lithium acetate or lithium benzoate. Successive reduction of the produced aldehydes with sodium borohydride (NaBH4) afforded the corresponding 1,3-diols in good to high yields in one-pot. Copyright

Synthesis and biological activity of cis 2-(6-chloropyridine-3-yl) methylamino-4-substitutedphenyl-5,5-dimethyl-1,3,2-dioxaphosphinane 2-oxides

De, Qing Shi,Liu, Yi,Feras,Xiao, Song Tan,Jian, Xin Chen

, p. 1937 - 1946 (2007/10/03)

A series of novel, asymmetric-cyclic phosphoramides containing substituted pyridine were synthesized via the condensation reactions of trans 2-chloro-4-substitutedphenyl-5, 5-dimethyl-1,3,2-dioxaphosphinane 2-oxide with 2-chloro-5-aminomethylpyridine or 3

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