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109027-55-6

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109027-55-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109027-55-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,0,2 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 109027-55:
(8*1)+(7*0)+(6*9)+(5*0)+(4*2)+(3*7)+(2*5)+(1*5)=106
106 % 10 = 6
So 109027-55-6 is a valid CAS Registry Number.

109027-55-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-(triphenylsilyloxy)-1-nonanol

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:109027-55-6 SDS

109027-55-6Downstream Products

109027-55-6Relevant articles and documents

Desilylation procedure via a naphthalene-catalysed lithiation reaction

Behloul, Cherif,Guijarro, David,Yus, Miguel

, p. 6908 - 6915 (2007/10/03)

The reaction of silyl protected alcohols, amines and thiols with lithium powder and a catalytic amount of naphthalene, in THF, at 0°C led, after hydrolysis, to the recovery of the free alcohols, amines and thiols in very good yields. At least a phenyl group was required in the silyl protecting group for the success of the reaction. Some polyfunctionalised starting materials have successfully been deprotected. The stereochemical outcome of the deprotection of a silylated chiral secondary alcohol has also been studied and no racemization was observed. The process has shown to be a good alternative to the acid-catalysed desilylation procedures, the latter being not useful for the deprotection of some silylated tertiary alcohols.

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