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Silane, ([1,1'-biphenyl]-2-yloxy)trimethyl-, is a chemical compound with the molecular formula C17H20OSi. It is an organosilicon compound, which means it contains silicon and carbon atoms bonded together. This specific compound features a trimethylsilyl group (Si(CH3)3) attached to a biphenyl-2-yloxy group, which is derived from a biphenyl molecule with an oxygen atom attached to the second carbon atom of one of the phenyl rings. The compound is known for its potential applications in the synthesis of various organic and organosilicon compounds, as well as in materials science for the development of new materials with unique properties. Due to its complex structure, it is typically used in specialized chemical research and industrial applications rather than in everyday products or consumer goods.

1022-21-5

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1022-21-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1022-21-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,2 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1022-21:
(6*1)+(5*0)+(4*2)+(3*2)+(2*2)+(1*1)=25
25 % 10 = 5
So 1022-21-5 is a valid CAS Registry Number.

1022-21-5SDS

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 trimethyl-(2-phenylphenoxy)silane

1.2 Other means of identification

Product number -
Other names trimethyl(biphenyl-2-yloxy)silane

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:1022-21-5 SDS

1022-21-5Relevant academic research and scientific papers

P/O ligand systems: Facile synthesis, structure, and catalytic tests of 2′-phosphanyl-1,1′-bipheny 1-2-ols and 2′-phosphanyl-1,1′-binaphthyl-2-ols

Kadyrov, Renat,Heinicke, Joachim,Kindermann, Markus K.,Heller, Detlef,Fischer, Christine,Selke, Ruediger,Fischer, Axel K.,Jones, Peter G.

, p. 1663 - 1670 (2007/10/03)

A facile synthesis of 2′-phosphanyl-1,1′-biphenyl- and 2′-phosphanyl-l,1′-binaphthyl-2-ols and their silyl ethers has been developed, consisting of electron-transfer-catalyzed ring-opening of dibenzofuran and dinaphthofuran, respectively, subsequent reaction with chlorophosphanes, and work-up with acetic acid or ClSiMe3. Studies of the molecular and crystal structures reveal the presence of P...H-O bridging bonds in the more basic /BuPhP derivative and a nearly perpendicular arrangement of the aryl planes in the biphenyl derivatives. The barrier to rotation of the aryl planes about the C-C axis was determined by NMR in the case of the P-asymmetric derivative 3d, using the appearance of diastereoisomers by atropisomerism and P-asymmetry. Comparative screening tests of the title compounds, phosphanylphenols and phosphanylnaphthols in homogeneous Rh-catalyzed reactions demonstrate catalytic activity in hydroformylation reactions and superior properties of the biphenyl- and binaphthyl-2-ol derivatives in relation to other P-O ligands. WILEY-VCH Verlag GmbH, 1997.

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