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2-(1-diethylcarbamoyl-ethyldisulfanyl)-N,N-diethyl-propionamide is a complex organic compound with the molecular formula C12H26N2O2S3. It is characterized by the presence of a disulfide bridge between two ethyl groups, a diethylcarbamoyl group, and a propionamide moiety. 2-(1-diethylcarbamoyl-ethyldisulfanyl)-N,N-diethyl-propionamide is a member of the sulfides class and is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. The compound's properties, such as its solubility and stability, can be influenced by the presence of the disulfide bond, which can undergo redox reactions. Its chemical structure and potential applications make it an interesting subject for research in the field of organic chemistry and drug development.

1907-80-8

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1907-80-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1907-80-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,0 and 7 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1907-80:
(6*1)+(5*9)+(4*0)+(3*7)+(2*8)+(1*0)=88
88 % 10 = 8
So 1907-80-8 is a valid CAS Registry Number.

1907-80-8Downstream Products

1907-80-8Relevant academic research and scientific papers

Dynamic kinetic resolution of amines involving biocatalysis and in situ free radical mediated racemization

Gastaldi, Stephane,Escoubet, Stephanie,Vanthuyne, Nicolas,Gil, Gerard,Bertrand, Michele P.

, p. 837 - 839 (2007)

(Chemical Equation Presented) The association of lipase-catalyzed enzymatic resolution with in situ racemization mediated with the thiyl radical enables the dynamic kinetic resolution of non-benzylic amines. It leads to (R)-amides with high enantioselectivities. It can be applied either to the conversion of racemic mixtures or to the inversion of (S)-enantiomers.

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