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56613-17-3

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56613-17-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56613-17-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,6,1 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 56613-17:
(7*5)+(6*6)+(5*6)+(4*1)+(3*3)+(2*1)+(1*7)=123
123 % 10 = 3
So 56613-17-3 is a valid CAS Registry Number.

56613-17-3SDS

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 trimethyl-[(4,7,7-trimethyl-3-bicyclo[2.2.1]hept-2-enyl)oxy]silane

1.2 Other means of identification

Product number -
Other names Campher-enoltrimethylsilylether

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:56613-17-3 SDS

56613-17-3Relevant articles and documents

Active Metals from Potassium-Graphite. Iron-Graphite as a New Debrominating Agent of vic-Dibromoalkanes and of α-Bromo Ketones

Savoia, Diego,Tagliavini, Emilio,Trombini, Claudio,Umani-Ronchi, Achille

, p. 876 - 879 (2007/10/02)

Iron-graphite (Fe-Gr), easily prepared by reduction of FeCl3 with potassium-graphite (C8K) in tetrahydrofuran, is conveniently used for the stereospecific debromination of vic-dibromoalkanes to alkenes and for the reductive debromination of α-bromo ketones to ketones in high yields.The latter reaction proceeds via Fe(II) enolates, which undergo deuteration, condensation, or O-silylation by reaction respectively with D2O, heptanal, or chlorotrimethylsilane.Moreover, the reaction of α,α'-dibromo ketones with Fe-Gr leads to 2-oxyallyl cations which can be trapped by suitable electron-rich olefins (enamines) or dienes (furan).

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