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(1E,3E,5E)-5-Methyl-1-phenylhepta-1,3,5-triene is an organic compound characterized by a conjugated diene system with a methyl group at the 5th carbon and a phenyl group at the 1st carbon. This molecule features a unique arrangement of double bonds (E,E,E), which means that all three double bonds are in the same geometric configuration, with the highest priority substituents on each double bond being on the same side of the molecule. The presence of the phenyl group imparts aromatic character, while the conjugated diene system allows for electronic delocalization, which can influence the compound's reactivity and stability. This specific geometric arrangement and the combination of aliphatic and aromatic moieties make (1E,3E,5E)-5-methyl-1-phenylhepta-1,3,5-triene an interesting compound for study in organic chemistry, particularly in the context of reactions involving conjugated systems and the effects of substituents on reactivity.

3893-06-9

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3893-06-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3893-06-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,9 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3893-06:
(6*3)+(5*8)+(4*9)+(3*3)+(2*0)+(1*6)=109
109 % 10 = 9
So 3893-06-9 is a valid CAS Registry Number.

3893-06-9Downstream Products

3893-06-9Relevant academic research and scientific papers

Synthetic Studies on Electron Transport Inhibitors. Part 2. Approaches to the Synthesis of Myxalamide D

Cox, Catherine M.,Whitting, Donald A.

, p. 1907 - 1911 (2007/10/02)

In a synthetic approach to ethyl myxalate-D 5 (X=OEt) the butendial monoacetals 12 and 15 were transformed by a Wadsworth-Emmons reaction and controlled hydrolysis into the (E,E)-aldehydoester (17); a Z-selective reaction with Bestmann's ylide 18 afforded

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