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19980-19-9

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19980-19-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19980-19-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,8 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 19980-19:
(7*1)+(6*9)+(5*9)+(4*8)+(3*0)+(2*1)+(1*9)=149
149 % 10 = 9
So 19980-19-9 is a valid CAS Registry Number.

19980-19-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-tert-butylcyclohexen-1-yl)oxy-trimethylsilane

1.2 Other means of identification

Product number -
Other names Silane,[[4-(1,1-dimethylethyl)-1-cyclohexen-1-yl]oxy]trimethyl

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:19980-19-9 SDS

19980-19-9Relevant articles and documents

Easy preparation of enoxysilanes from aldehydes and ketones catalyzed by samarium diiodide

Hydrio, Jerome,Van De Weghe, Pierre,Collin, Jacqueline

, p. 68 - 72 (1997)

Ketones and α-substituted aldehydes are converted to trimethylsilyl enol ethers by reaction with the trimethylsilyl ketene acetal of methyl isobutyrate in dichloromethane in presence of a catalytic amount of samarium diiodide.

Halogenative difluorohomologation of ketones

Fedorov, Oleg V.,Kosobokov, Mikhail D.,Levin, Vitalij V.,Struchkova, Marina I.,Dilman, Alexander D.

, p. 5870 - 5876 (2015/06/16)

A method for the difluorohomologation of ketones accompanied by halogenation of a C-H bond is described. The reaction involves silylation, difluorocarbene addition using Me3SiCF2Br activated by a bromide ion, and halogenation of intermediate cyclopropanes with N-bromo- or N-iodosuccinimide. The whole process is performed without isolation of intermediates. The resulting α,α-difluoro-β-halo-substituted ketones can be readily converted into fluorine containing pyrazole derivatives and oxetanes.

Enantioselective desymmetrization of prochiral ketones via an organocatalytic deprotonation process

Claraz, Aurelie,Oudeyer, Sylvain,Levacher, Vincent

, p. 764 - 768 (2013/07/25)

The first desymmetrization of 4-substituted cyclohexanones by organocatalytic asymmetric deprotonation at low catalyst loading is reported. The combination of N,O-bis(trimethylsilyl)acetamide (BSA) and chiral quaternary ammonium aryloxide salts has been u

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