Welcome to LookChem.com Sign In|Join Free
  • or
(E)-1-Phenyl-but-1-en-1-ol, also known as 1-phenyl-1-buten-3-ol or cinnamyl alcohol, is an organic compound with the molecular formula C10H12O. It is a colorless to pale yellow liquid with a strong, sweet, floral odor. This chemical is a chiral molecule, with the (E)-isomer being the most common and commercially available form. It is widely used in the fragrance industry, particularly in the production of perfumes and colognes, due to its pleasant scent. Additionally, it is employed as a flavoring agent in food and beverages, imparting a sweet, balsamic taste. Cinnamyl alcohol is also used in the synthesis of various pharmaceuticals and chemical intermediates. It is derived from the essential oils of cinnamon and other plants, and can be synthesized through various chemical processes, including the condensation of benzaldehyde with acetaldehyde.

6052-55-7

Post Buying Request

6052-55-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

6052-55-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6052-55-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,5 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6052-55:
(6*6)+(5*0)+(4*5)+(3*2)+(2*5)+(1*5)=77
77 % 10 = 7
So 6052-55-7 is a valid CAS Registry Number.

6052-55-7Upstream product

6052-55-7Downstream Products

6052-55-7Relevant academic research and scientific papers

Is the McLafferty Rearrangement of Ketones Concerted or Stepwise? The Application of Kinetic Isotope Effects

Stringer, Michael B.,Underwood, Dennis J.,Bowie, John H.,Allison, Colin E.,Donchi, Kevin F.,Derrick, Peter J.

, p. 270 - 276 (2007/10/02)

Intramolecular 13C and 2H isotope effects have been measured for unimolecular losses of ethene (the McLafferty rearrangement) from metastable molecular ions of 2-ethyl-1-phenylbutan-1-one, 3-ethylpentan-2-one and heptan-4-one.Primary and secondary deuterium isotope effects are observed at the γ-(terminal) and β-positions, respectively.Large primary 13C isotope effects occur at β-positions and for the γ positions of 3-ethylpentan-2-one and heptan-4-one.The carbon isotope effects in the cases of the doubly isotopically labelled CH3COCH(C2H5)((13)CH2CH3) and CD3COCD(C2D5)((13)CD2CD3) are 1.17 (+/-0.01) and 1.04 (+/-0.01), respectively.All of these isotope effects are consistent with a stepwise mechanism in which more than one step is rate determining.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 6052-55-7