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4-methyl-1,2-diphenylpentan-1-one is an organic compound with the molecular formula C18H22O. It is a ketone derivative characterized by a five-carbon chain with a methyl group at the fourth carbon, and two phenyl rings attached to the first and second carbons. This chemical is known for its potential applications in the synthesis of various pharmaceuticals and fragrances due to its unique structure and reactivity. It is typically synthesized through chemical reactions involving the condensation of appropriate precursors, such as aldehydes and ketones, and can be further functionalized to create a range of derivatives. The compound is of interest in organic chemistry for its ability to participate in various types of reactions, including reduction, oxidation, and substitution, making it a versatile building block in the creation of more complex molecules.

3326-48-5

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3326-48-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3326-48-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,2 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3326-48:
(6*3)+(5*3)+(4*2)+(3*6)+(2*4)+(1*8)=75
75 % 10 = 5
So 3326-48-5 is a valid CAS Registry Number.

3326-48-5Downstream Products

3326-48-5Relevant academic research and scientific papers

Catalytic asymmetric cross-couplings of racemic α-bromoketones with arylzinc reagents

Lundin, Pamela M.,Esquivias, Jorge,Fu, Gregory C.

supporting information; experimental part, p. 154 - 156 (2009/04/07)

(Chemical Equation Presented) Nickel box: The first catalytic asymmetric method for cross-coupling arylzinc reagents with α-bromoketones has been developed (see scheme). This stereoconvergent carbon-carbon bond-forming process occurs under unusually mild conditions and without activators, thereby allowing the generation of potentially labile tertiary stereocenters.

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