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N-(9-Anthracenemethyl)cinchoniumbromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

365567-24-4

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365567-24-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 365567-24-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,5,5,6 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 365567-24:
(8*3)+(7*6)+(6*5)+(5*5)+(4*6)+(3*7)+(2*2)+(1*4)=174
174 % 10 = 4
So 365567-24-4 is a valid CAS Registry Number.

365567-24-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(anthracen-9-ylmethyl)cinchoninium bromide

1.2 Other means of identification

Product number -
Other names -

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:365567-24-4 SDS

365567-24-4Downstream Products

365567-24-4Relevant academic research and scientific papers

Ring-Strain-Enabled Catalytic Asymmetric Umpolung C-O Bond-Forming Reactions of 1,2-Oxazetidines for the Synthesis of Functionalized Chiral Ethers

Wu, Binyu,Yang, Jinggang,Gao, Min,Hu, Lin

supporting information, p. 5561 - 5566 (2020/07/14)

An unprecedented catalytic asymmetric umpolung C-O bond-forming reaction of N-nosyl 1,2-oxazetidines with β-keto esters has been achieved in the presence of a chiral phase-transfer catalyst, allowing access to a range of highly functionalized chiral ethers bearing quaternary and no adjacent stereogenic centers with high yields, excellent enantioselectivities, and diastereoselectivities (up to 97percent ee and 20:1 dr). These versatile products could be flexibly transformed into biologically important chiral fused and spiro morpholines in two steps.

Asymmetric α-alkylation of cyclic β-keto esters and β-keto amides by phase-transfer catalysis

Wang, Yakun,Li, Yueyun,Lian, Mingming,Zhang, Jixia,Liu, Zhaomin,Tang, Xiaofei,Yin, Hang,Meng, Qingwei

supporting information, p. 573 - 584 (2019/01/24)

Without employing any transition metal, a highly enantioselective α-alkylation of cyclic β-keto esters and β-keto amides has been realized by phase-transfer catalysis. This improved procedure is applicable to different kinds of halides with cinchona derivatives and gives the corresponding products in excellent enantiopurities (up to 98% ee) and good yields (up to 98%). Moreover, the reaction was scalable and the phase-transfer catalyst was recyclable. This provided an alternative and competitive method to the asymmetric α-alkylation of β-dicarbonyl compounds.

Asymmetric direct α-hydroxylation of β-Oxo esters by phase-transfer catalysis using chiral quaternary ammonium salts

Lian, Mingming,Li, Zhi,Du, Jian,Meng, Qingwei,Gao, Zhanxian

supporting information; experimental part, p. 6525 - 6530 (2011/02/25)

The first enantioselective direct α-hydroxylation of β-oxo esters was developed by using phase-transfer catalysis. 1-Indanone-derived 1-adamantyl (1-Ad) β-oxo esters, in the presence of commercially available cumyl hydroperoxide and a cinchonine-based ammonium salt, resulted in the corresponding products with 69-91 % yield and 65-74 % ee. The reaction had also been successfully scaled-up to a gram quantity, and a similar yield was obtained without loss of the enantioselectivity. Copyright

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