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105966-41-4

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105966-41-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105966-41-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,9,6 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 105966-41:
(8*1)+(7*0)+(6*5)+(5*9)+(4*6)+(3*6)+(2*4)+(1*1)=134
134 % 10 = 4
So 105966-41-4 is a valid CAS Registry Number.

105966-41-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl-diphenyl-(2-phenylethoxy)silane

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:105966-41-4 SDS

105966-41-4Relevant articles and documents

N-heterocyclic carbene organocatalysts for dehydrogenative coupling of silanes and hydroxyl compounds

Gao, Dongjing,Cui, Chunming

, p. 11143 - 11147 (2013)

Go organic! N-Heterocyclic carbene (NHC) 1,3-diisopropyl-4,5- dimethylimidazol-2-ylidene (IiPr) has been found to be an efficient and selective catalyst for the dehydrogenative coupling of a wide range of silanes and hydroxyl groups to form Si-O bonds under mild and solvent-free conditions (see scheme). Mechanistic studies indicated that the activation of hydroxyl groups by the NHC is the most plausible initial step for the process. Copyright

Versatile dehydrogenative alcohol silylation catalyzed by Cu(I)-phosphine complex

Ito, Hajime,Watanabe, Akiko,Sawamura, Masaya

, p. 1869 - 1871 (2005)

(Chemical Equation Presented) Cu(I) complexes of xanthane-based diphosphines were versatile catalysts for dehydrogenative alcohol silylation, exhibiting high activity and broad substrate scope. Highly selective silylation of 1-decanol over 2-decanol is possible even with a silylating reagent of small steric demand such as HSiMe2Ph or HSiEt3.

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