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220565-63-9

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220565-63-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 220565-63-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,5,6 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 220565-63:
(8*2)+(7*2)+(6*0)+(5*5)+(4*6)+(3*5)+(2*6)+(1*3)=109
109 % 10 = 9
So 220565-63-9 is a valid CAS Registry Number.

220565-63-9SDS

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 3-pyridylzinc bromide

1.2 Other means of identification

Product number -
Other names 3-pyridinylzinc bromide

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:220565-63-9 SDS

220565-63-9Relevant articles and documents

Fukuyama Cross-Coupling Approach to Isoprekinamycin: Discovery of the Highly Active and Bench-Stable Palladium Precatalyst POxAP

Tang, Shuang-Qi,Bricard, Jacques,Schmitt, Martine,Bihel, Frédéric

supporting information, p. 844 - 848 (2019/01/30)

An efficient and user-friendly palladium(II) precatalyst, POxAP (post-oxidative-addition precatalyst), was identified for use in Fukuyama cross-coupling reactions. Suitable for storage under air, the POxAP precatalyst allowed reaction between thioesters and organozinc reagents with turnover numbers of ~90000. A series of 23 ketones were obtained with yields ranging from 53 to 99%. As proof of efficacy, an alternative approach was developed for the synthesis of a key precursor of the natural product isoprekinamycin.

Cobalt-Catalyzed Formation of 2-Pyridylzinc Reagents and Their Subsequent Coupling

Linke, Stephanie,Manolikakès, Sofia M.,Auffrant, Audrey,Gosmini, Corinne

, p. 2595 - 2600 (2018/06/08)

The preparation of pyridylzinc compounds from the corresponding pyridyl halides using a cobalt catalyst is described. The complex employed features a polydentate N-heterocyclic ligand and allows the reaction to be carried out in the absence of pyridine as

A versatile organozinc approach to the synthesis of potential organic functional building blocks: 5-substituted 3-bromo-2-methylthiophene derivatives

Cheon, Jong-Woo,Cho, Hyun-Hee,Kim, Seung-Hoi

, p. 1266 - 1269 (2015/07/15)

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