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20606-25-1

20606-25-1

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20606-25-1 Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 70, p. 3352, 1948 DOI: 10.1021/ja01190a040

Check Digit Verification of cas no

The CAS Registry Mumber 20606-25-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,6,0 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 20606-25:
(7*2)+(6*0)+(5*6)+(4*0)+(3*6)+(2*2)+(1*5)=71
71 % 10 = 1
So 20606-25-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H20O3/c13-11(8-4-5-9-12(14)15)10-6-2-1-3-7-10/h10H,1-9H2,(H,14,15)

20606-25-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-CYCLOHEXYL-6-OXOHEXANOIC ACID

1.2 Other means of identification

Product number -
Other names 1-Oxo-1-cylohexyl-hexansaeure-(6)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:20606-25-1 SDS

20606-25-1Relevant articles and documents

Azolium/Hydroquinone Organo-Radical Co-Catalysis: Aerobic C?C-Bond Cleavage in Ketones

Nakatsuji, Yuya,Kobayashi, Yusuke,Masuda, Sakyo,Takemoto, Yoshiji

supporting information, p. 2633 - 2637 (2021/02/03)

Organo-radical catalysts have recently attracted great interest, and the development of this field can be expected to broaden the applications of organocatalysis. Herein, the first example of a radical-generating system is reported that does not require any photoirradiation, radical initiators, or preactivated substrates. The oxidative C?C-bond cleavage of 2-substituted cyclohexanones was achieved using an azolium salt and a hydroquinone as co-catalysts. A catalytic mechanism was proposed based on the results of diffusion-ordered spectroscopy and cyclic voltammetry measurements, as well as computational studies.

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