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19096-89-0

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19096-89-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19096-89-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,9 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 19096-89:
(7*1)+(6*9)+(5*0)+(4*9)+(3*6)+(2*8)+(1*9)=140
140 % 10 = 0
So 19096-89-0 is a valid CAS Registry Number.

19096-89-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (methoxymethylene)cyclohexane

1.2 Other means of identification

Product number -
Other names methoxymethylelecyclohexanone

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:19096-89-0 SDS

19096-89-0Relevant articles and documents

Antimalarial effect of 3-methoxy-1,2-dioxetanes on the erythrocytic cycle of Plasmodium falciparum

Lopes, Nicolas S.,Yoshitake, Ariane M.,Silva, Adriana F.,Oliveira, Vani X.,Silva, Leandro S.,Pinheiro, Ana A. S.,Ciscato, Luiz Francisco M. L.

, p. 1373 - 1377 (2015)

The antimalarial activity of peroxides most likely originates from their interaction with iron(II) species located inside the malaria parasite, which forms destructive radical species through a Fenton-like mechanism. This article reports the first evaluat

Practical preparation of methyl vinyl ethers through the direct coupling of ketones with CHCl2OMe promoted by Mg/TiCl4/THF

Ananthan, Bakthavachalam,Yan, Tu-Hsin

supporting information, p. 753 - 760 (2018/03/12)

Herein we utilized a new methylene carbenoid as an extremely simple and highly practical reagent for the preparation of vinyl ether with good to excellent yield. This method efficiently effects methoxymethylenation or vinyl ether formation of enolizable, nonenolizable, and sterically hindered ketones. The complexation of Ti–Mg–CHOMe was facilitated, presumably, by THF dramatically increasing the feasibility; and scope of this protocol is to produce vinyl ethers which can be used as convenient building blocks for the preparation of biologically useful molecules.

Silica-immobilized chiral dirhodium(II) catalyst for enantioselective carbenoid reactions

Chepiga, Kathryn M.,Feng, Yan,Brunelli, Nicholas A.,Jones, Christopher W.,Davies, Huw M. L.

supporting information, p. 6136 - 6139 (2014/01/17)

A silica-supported dirhodium(II) tetraprolinate catalyst was synthesized in four steps from l-proline and used in a range of enantioselective transformations of donor/acceptor carbenoids. These include cyclopropenation, cyclopropanation, tandem ylide form

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