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(E)-1-phenyl-4-propyl-1-hepten-4-ol is a complex organic compound with the molecular formula C17H24O. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it belongs to the class of alkenes due to the presence of a carbon-carbon double bond. (E)-1-phenyl-4-propyl-1-hepten-4-ol features a phenyl group (C6H5) attached to the first carbon, a propyl group (C3H7) at the fourth carbon, and a hydroxyl group (-OH) at the fourth carbon as well, which gives it its alcohol functionality. The "E" configuration indicates that the phenyl and propyl groups are on opposite sides of the double bond when viewed from the perspective of the highest priority substituent. (E)-1-phenyl-4-propyl-1-hepten-4-ol is likely to be found in the fragrance and flavor industry due to its potential aromatic properties, and it may also have applications in the synthesis of more complex organic molecules.

55552-41-5

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55552-41-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55552-41-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,5,5 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 55552-41:
(7*5)+(6*5)+(5*5)+(4*5)+(3*2)+(2*4)+(1*1)=125
125 % 10 = 5
So 55552-41-5 is a valid CAS Registry Number.

55552-41-5Downstream Products

55552-41-5Relevant academic research and scientific papers

Samarium(II)-mediated reaction of allylic phosphate esters with carbonyl compounds: A new method for "Umpolung" of allylic phosphates

Araki, Shuki,Hatano, Masahiro,Ito, Hirokazu,Butsugan, Yasuo

, p. 329 - 336 (2007/10/02)

Allylic phosphates allylate ketones and aldehydes in the presence of samarium(II) iodide.The coupling proceeds with the preservation of the olefin geometry ever, regio- and stereoselectivity are not high.

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