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(4-Bromo-phenyl)-acetaldehyde oxime is an organic compound with the chemical formula C8H7BrNO. It is derived from acetaldehyde, where one of the hydrogen atoms is replaced by a 4-bromophenyl group, and the aldehyde group is converted to an oxime. (4-Bromo-phenyl)-acetaldehyde oxime is a colorless to pale yellow liquid and is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. It is characterized by its bromine atom attached to the phenyl ring, which imparts unique chemical properties and reactivity. The oxime functional group gives it the ability to participate in various chemical reactions, making it a valuable building block in organic synthesis.

4410-19-9

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4410-19-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4410-19-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,1 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4410-19:
(6*4)+(5*4)+(4*1)+(3*0)+(2*1)+(1*9)=59
59 % 10 = 9
So 4410-19-9 is a valid CAS Registry Number.

4410-19-9Downstream Products

4410-19-9Relevant academic research and scientific papers

Gold catalysts open a new general chemoselective route to synthesize oximes by hydrogenation of α,β-unsaturated nitrocompounds with H 2

Corma, Avelino,Serna, Pedro,Garcia, Hermenegildo

, p. 6358 - 6359 (2007)

The unprecedented chemoselective reduction of α,β-unsaturated nitroalkenes to oximes using hydrogen has been achieved with gold nanoparticles supported on TiO2. In contrast to the excellent catalytic performance of gold, related palladium and platinum catalysts are unselective, leading to the reduction of C=C double bond as well as the reduction of the NO2 to NH2. The selectivity of Au/TiO2 for the formation of oximes opens the way for the general use of the Henry reaction in organic synthesis. Copyright

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