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Cyclooctanone, 2-(2-oxo-2-phenylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62369-04-4

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62369-04-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62369-04-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,3,6 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 62369-04:
(7*6)+(6*2)+(5*3)+(4*6)+(3*9)+(2*0)+(1*4)=124
124 % 10 = 4
So 62369-04-4 is a valid CAS Registry Number.

62369-04-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenacylcyclooctan-1-one

1.2 Other means of identification

Product number -
Other names 2-phenacylcyclooctanone

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:62369-04-4 SDS

62369-04-4Downstream Products

62369-04-4Relevant academic research and scientific papers

NEW GENERAL SYNTHESIS OF MEDIUM RING-LACTONES VIA A REGIOSELECTIVE β-SCISSION OF ALKOXYL RADICALS GENERATED FROM CATACONDENSED LACTOLS

Suginome, Hiroshi,Yamada, Shinji

, p. 3371 - 3386 (2007/10/02)

We describe a new general method for the synthesis of medium-sized lactones based on ring-enlargement via a regioselective β-scission of alkoxyl radicals generated by photolysis from the hypoiodites of several catacondensed lactols.The syntheses of 9-membered lactones from 6/5 fused lactols, 10-menbered lactones including a naturally occuring lactone, phoracantholide I, from 6/6 or 7/5 fused lactols, and 11-membered lactones from 7/6 or 8/5 fused lactols are shown to be achieved by the present method.This new method may have a potential for application to the synthesis of either smaller or larger-sized lactones.

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