Welcome to LookChem.com Sign In|Join Free
  • or
2-(2-(1,3-dioxolane))cyclohexanone is a complex organic compound with the molecular formula C9H14O3. It is a cyclic ketone derivative, featuring a cyclohexanone ring with a 1,3-dioxolane group attached to the 2-position. The 1,3-dioxolane group is a five-membered ring containing two oxygen atoms, which contributes to the compound's unique chemical properties. 2-(2-(1,3-dioxolane))cyclohexanone is primarily used in the synthesis of various pharmaceuticals and agrochemicals due to its versatile chemical structure and reactivity. It is an intermediate in the production of certain drugs and can also be used as a solvent or a reagent in organic synthesis. The compound's stability and reactivity make it a valuable component in the development of new chemical entities.

5687-00-3

Post Buying Request

5687-00-3 Suppliers

Recommended suppliers

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

5687-00-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5687-00-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,8 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5687-00:
(6*5)+(5*6)+(4*8)+(3*7)+(2*0)+(1*0)=113
113 % 10 = 3
So 5687-00-3 is a valid CAS Registry Number.

5687-00-3Relevant academic research and scientific papers

FORMATION AND CHARACTERIZATION OF TETRABUTYLAMMONIUM SULFATE RADICAL: APPLICATION TO ORGANIC SYNTHESIS

Kim, Yong Hae,Jung, Jae Chul,Choi, Hyun Chul

, p. 431 - 434 (2007/10/02)

n-Tetrabutylammonium Peroxydisulfate has been successfully synthesized and turned out to be a sulfate radical source which can be utilized for the efficient organic syntheses: chemoselective oxidations of alcohols to ketones, 2-tetrahydrofuranylation of a

Acylketene acetals in organic synthesis

Eid Jr.,Konopelski

, p. 975 - 992 (2007/10/02)

The preparation and reactivity of achiral and enantiomerically pure acylketene acetals are described. The key reactions of these substrates involve facile conjugate hydroboration and organolithium addition. Enantiomerically pure acylketene acetals were employed to generate a homochiral β-keto ketal through a highly diastereoselective lithium enolate quench. This β-ketal, which was also prepared through a desymmetrization ketalization reaction on a meso dione, was employed in the synthesis of the insect pheromone sitophilure.

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 5687-00-3