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Butyl-1,1-d2-triphenylphosphonium bromide is a chemical compound with the molecular formula C26H28BrD2P. It is a derivative of triphenylphosphonium bromide, where two hydrogen atoms in the butyl group are replaced by deuterium atoms (D2). butyl-1,1-d2-triphenylphosphonium bromide is often used in organic synthesis and as a reagent in various chemical reactions. It is a colorless solid that is soluble in organic solvents. The presence of deuterium atoms makes it useful in studies involving isotope labeling and in applications where the incorporation of deuterium can provide insights into reaction mechanisms or improve the stability of the compound.

1779-50-6

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1779-50-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1779-50-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,7 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1779-50:
(6*1)+(5*7)+(4*7)+(3*9)+(2*5)+(1*0)=106
106 % 10 = 6
So 1779-50-6 is a valid CAS Registry Number.

1779-50-6Downstream Products

1779-50-6Relevant academic research and scientific papers

Reaction of thiolesters with nitrogen ylides

Voltrova, Svatava,Srogl, Jiri

, p. 1677 - 1679 (2008)

The pairing of unstabilized nitrogen ylides generated in situ with functionalized thiolesters under ambient conditions resulted in a new intramolecular carbon-carbon bond forming reaction. The scope of the reaction was illustrated with a series of substit

STEREOCHEMICAL OBSERVATIONS ON THE WITTIG REACTION OF OXIDO PHOSPHONIUM YLIDES WITH ALDEHYDES

Maryanoff, Bruce E.,Reitz Allen B.,Duhl-Emswiler, Barbara A.

, p. 2477 - 2480 (2007/10/02)

The reaction of aldehydes with oxido ylides shows a dramatic dependence of alkene stereochemistry on the distance between oxygen and phosphorus atoms; ylides with proximal O and P atoms favor production of E alkenes.The high E stereoselectivity with γ-oxido ylides is not mainly attributable to intramolecular proton-exchange in a Wittig intermediate.

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