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1-Azabicyclo[2.2.2]octan-3-one, 2-[(4-methoxyphenyl)methylene]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52407-93-9

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52407-93-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52407-93-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,4,0 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 52407-93:
(7*5)+(6*2)+(5*4)+(4*0)+(3*7)+(2*9)+(1*3)=109
109 % 10 = 9
So 52407-93-9 is a valid CAS Registry Number.

52407-93-9SDS

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-[(4-methoxyphenyl)methylidene]-1-azabicyclo[2.2.2]octan-3-one

1.2 Other means of identification

Product number -
Other names 1-Azabicyclo[2.2.2]octan-3-one,2-[(4-methoxyphenyl)methylene]

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:52407-93-9 SDS

52407-93-9Relevant academic research and scientific papers

Ruthenium-Catalyzed Highly Enantioselective Synthesis of cis-3-Quinuclidinols via DKR Asymmetric Transfer Hydrogenation

Luo, Zhonghua,Wang, Zhongqing,Sun, Guodong,Jian, Weilin,Jiang, Fengkai,Luan, Baolei,Li, Ridong,Zhang, Lei

supporting information, p. 4322 - 4326 (2020/06/04)

A method for the enantioselective synthesis of cis-3-quinuclidinols by Ru-catalyzed asymmetric transfer hydrogenation via dynamic kinetic resolution is described. The reaction proceeded under mild conditions using ammonium formate as the hydrogen donor, affording the products in high yields (up to 99%) with excellent diastereoselectivity (up to 99:1 dr) and enantioselectivity (95-99% ee). This protocol was applicable to gram-scale preparation with perfect enantioselectivity through simple recrystallization.

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