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3,3,3-triphenylpropionic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

50354-49-9

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50354-49-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50354-49-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,3,5 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 50354-49:
(7*5)+(6*0)+(5*3)+(4*5)+(3*4)+(2*4)+(1*9)=99
99 % 10 = 9
So 50354-49-9 is a valid CAS Registry Number.

50354-49-9Relevant academic research and scientific papers

Aminolysis of allyl esters with bislithium aryl amides

Faler, Catherine A.,Joullié, Madeleine M.

, p. 7229 - 7231 (2006)

The aminolysis of allyl esters with bislithium amides is reported. Tertiary aryl amides were synthesized in a one-pot reaction with bislithium amides and a suitable electrophile in good yields. The scope of this reaction was demonstrated with a variety of anilines and aminopyridines and applied to the synthesis of triphenylmethylacetamides.

Synthesis and preliminary characterization of some polyester rotaxanes

Gibson, Harry W.,Liu, Shu,Lecavalier, Pierre,Wu, Charles,Shen, Ya Xi

, p. 852 - 872 (2007/10/02)

A series of polyester rotaxanes containing polysebacate backbones [decamethylene, tri(ethyleneoxy), and 1,4-butylene] and ethylene oxide-based crown ethers [30-crown-10,42-crown-14, 60-crown-20, and bis(p-phenylene)-34-crown-10] was synthesized via step growth polymerizations using diacid chloride-diol and transesterification reactions. The polyrotaxanes were purified by multiple reprecipitations in good solvents for the crown ethers, and the physical linkage of the crown ether to the polymeric backbone was confirmed by a variety of experiments, including hydrolysis, NMR, GPC, and VPO. Up to 55 wt % macrocycle was incorporated, depending on the size and shape of the macrocycle and the feed ratios employed. In all cases, the solubilities of the polyrotaxanes were strongly influenced by the cyclic component; enhanced solubilities in polar solvents were observed relative to the simple parent polysebacates. Mark-Houwink K and a values were also strongly affected by rotaxane formation; in the case most thoroughly investigated, K decreased by almost 2 orders of magnitude and a doubled. Interpretation of this observation is complicated by the changes in solubility. Thermal behavior was also affected. In the tri-(ethyleneoxy) system, Tg is lowered in the rotaxanes; in the 60-crown-20 system, the macrocycle crystallized! The poly(butylene sebacate) 60-crown-20 and 42-crown-14 systems also possessed two crystalline phases, a crown ether phase and a poly(butylene sebacate) phase. These exciting result demonstrate the mobility of the macrocycle along the polyester backbone in melt and solution states, allowing aggregation and crystallization without dethreading.

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