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120569-12-2

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120569-12-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120569-12-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,5,6 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 120569-12:
(8*1)+(7*2)+(6*0)+(5*5)+(4*6)+(3*9)+(2*1)+(1*2)=102
102 % 10 = 2
So 120569-12-2 is a valid CAS Registry Number.

120569-12-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-Dichloro-2-cyclohexen-1-one

1.2 Other means of identification

Product number -
Other names 2,3-dichlorocyclohex-2-enone

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:120569-12-2 SDS

120569-12-2Downstream Products

120569-12-2Relevant articles and documents

AuFeAg hybrid nanoparticles as an efficient recyclable catalyst for the synthesis of α,β- and β,β-dichloroenones

Mishra, Kanchan,Basavegowda, Nagaraj,Lee, Yong Rok

, p. 180 - 187 (2015)

A facile and green pioneer approach for the synthesis of stable trimetallic AuFeAg hybrid nanoparticles is described. This synthetic method is green-chemistry compatible and totally free of additives. The particle shape and size, surface chemistry, crystallinity, elemental composition, thermal and magnetic properties were investigated. The catalytic performance of the synthesized nanoparticles is also described. The hybrid nanocatalyst exhibited strong catalytic activity for the synthesis of α,β- and β,β-dichloroenones, which are important synthetic intermediates in the preparation of natural products. The reason behind the catalytic performance of nano sized hybrid particles was attributed to their high specific surface area. In addition, the nanocatalyst was easy to separate from the reaction mixture using an external magnet and could be reused for five consecutive reactions without any significant loss of activity. Using the present method, the trimetallic hybrid combination can be designed for similar types of catalytic reactions.

Ruthenium(II)-catalyzed protocol for preparation of diverse α,β- and β,β-Dihaloenones from diazodicarbonyls

Magar, Krishna Bahadur Somai,Lee, Yong Rok

, p. 3422 - 3432 (2015/02/02)

Efficient one-step syntheses of α,β- and β,β-dihaloenones were achieved by ruthenium(II)- catalyzed reactions between cyclic or acyclic diazodicarbonyl compounds and oxalyl chloride or oxalyl bromide in moderate to good yields. This methodology offers sev

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