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96248-16-7

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96248-16-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96248-16-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,2,4 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 96248-16:
(7*9)+(6*6)+(5*2)+(4*4)+(3*8)+(2*1)+(1*6)=157
157 % 10 = 7
So 96248-16-7 is a valid CAS Registry Number.

96248-16-7Relevant academic research and scientific papers

Synthesis and in vitro reactivity of 3-carbamoyl-2- phenylpropionaldehyde and 2-phenylpropenal: Putative reactive metabolites of felbamate

Thompson, Charles D.,Kinter, Michael T.,Macdonald, Timothy L.

, p. 1225 - 1229 (2007/10/03)

We propose that 3-carbamoyl-2-phenylpropionaldehyde is an intermediate in the metabolism of felbamate, an anti-epileptic drug with a unique profile of therapeutic activity, and undergoes a cascade of chemical reactions responsible for the toxic properties of the parent drug. To test this hypothesis, we have synthesized 3-carbamoyl-2-phenylpropionaldehyde and evaluated its in vitro reactivity. This molecule was found to be highly unstable at physiological pH (t(1/2) ≤ 30 s) and to undergo facile elimination to 2-phenylpropenal, an α, β-unsaturated aldehyde commonly termed atropaldehyde. However, the predominant reaction pathway for 3- carbamoyl-2-phenylpropionaldehyde was reversible cyclization to generate 4- hydroxy-5-phenyltetrahydro-1,3-oxazin-2-one, a urethane that has a considerably longer half-life at physiological pH (t(1/2) ≤ 5 h) and may serve as a stable reservoir of the reactive aldehyde both in vitro and in vivo. Atropaldehyde is a potent electrophile and was found to exhibit cytotoxicity to cultured fibroblasts (50% growth inhibition (GI50) = 4.1 ± 1.1 μM) comparable to the known unsaturated aldehyde toxins, 4-hydroxy-2- nonenal and acrolein. 3-Carbamoyl-2-phenylpropionaldehyde also exhibited significant cytotoxicity (GI50 = 53 ± 8 μM), whereas 2-phenyl-1, 3- propanediol monocarbamate (GI50 > 500 μM) and 3-carbamoyl-2- phenylpropionic acid (GI50 > 500 μM) were nontoxic. We have additionally demonstrated the formation of a glutathione-atropaldehyde conjugate from the in vitro incubation of 3-carbamoyl-2-phenylpropionaldehyde with glutathione. Thus, the potent cytotoxicity and potential allergenicity of atropaldehyde implicate this unsaturated aldehyde as a possible causative agent in the toxicities observed with felbamate treatment.

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