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69983-36-4

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69983-36-4 Usage

General Description

Bis(4-methoxyphenyl)dimethylsilane, 97% is a chemical compound that consists of two 4-methoxyphenyl groups attached to a dimethylsilane moiety. Bis(4-methoxyphenyl)dimethylsilane, 97% is commonly used as a crosslinking agent in the production of silicone polymers and as a protective agent for various materials. With a purity of 97%, this chemical is highly efficient in its intended applications and is known for its stability and reactivity. Additionally, it is important to handle this compound with proper safety precautions, as it may be hazardous if mishandled or not used in accordance with its specified guidelines.

Check Digit Verification of cas no

The CAS Registry Mumber 69983-36-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,9,8 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 69983-36:
(7*6)+(6*9)+(5*9)+(4*8)+(3*3)+(2*3)+(1*6)=194
194 % 10 = 4
So 69983-36-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H20O2Si/c1-17-13-5-9-15(10-6-13)19(3,4)16-11-7-14(18-2)8-12-16/h5-12H,1-4H3

69983-36-4 Well-known Company Product Price

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  • Alfa Aesar

  • (H28045)  Bis(4-methoxyphenyl)dimethylsilane, 97%   

  • 69983-36-4

  • 1g

  • 594.0CNY

  • Detail
  • Alfa Aesar

  • (H28045)  Bis(4-methoxyphenyl)dimethylsilane, 97%   

  • 69983-36-4

  • 5g

  • 1666.0CNY

  • Detail

69983-36-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(4-methoxyphenyl)-dimethylsilane

1.2 Other means of identification

Product number -
Other names Silane,bis(4-methoxyphenyl)dimethyl-(9CI)

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:69983-36-4 SDS

69983-36-4Downstream Products

69983-36-4Relevant articles and documents

METHOD FOR PRODUCING ARYLSILANE COMPOUND CONTAINING HALOSILANE COMPOUND AS RAW MATERIAL

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Paragraph 0059-0063, (2020/03/06)

PROBLEM TO BE SOLVED: To provide a method for producing an arylsilane compound with low production cost. SOLUTION: A method for producing an arylsilane compound includes a reaction step for the cross-coupling reaction of a halosilane compound represented by general formula (A-1), (A-2), or (A-3) and an arylboronic acid pinacol ester in the presence of a nickel catalyst, a Lewis acid catalyst, and an organic base (R independently represent an aromatic hydrocarbon group, a heteroaromatic ring group, or a C1-20 hydrocarbon group; X independently represent a halogeno group or a trifluoromethanesulfonyloxy group). SELECTED DRAWING: None COPYRIGHT: (C)2020,JPOandINPIT

New Diphosphane Ligands Based on Bisphenol A Backbones - Synthesis and Coordination Chemistry

Van Der Vlugt, Jarl Ivar,Grutters, Michiel M. P.,Mills, Allison M.,Kooijman, Huub,Spek, Anthony L.,Vogt, Dieter

, p. 4361 - 4369 (2007/10/03)

A series of easily accessible diphosphane compounds 1-4, based on bisphenol A derived backbones, has been prepared. A straightforward two-step synthetic route has been employed to obtain these new ligands in good yields from cheap starting materials. Mole

Transmission of electronic effects via a SiMe2 spacer in 4-mono- and 4,4'-disubstituted diphenyldimethylsilanes: 29Si and 13C NMR spectroscopy and PM3 semi-empirical calculations

Walree, Cornelis A. van,Lauteslager, Xavier Y.,Wageningen, Andreas M. A. van,Zwikker, Jan W.,Jenneskens, Leonardus W.

, p. 117 - 126 (2007/10/02)

Some 29Si and 13C NMR studies were performed of series of 4-substituted phenyltrimethylsilanes and 4-substituted and 4,4'-disubstituted diphenyldimethylsilanes.Within each series linear relationships are found between the chemical shifts and (a) the Hammett substituent constants ?p and (b) the PM3-calculated total atomic charges.It is inferred that the SiMe2 ?-type spacer weakly mediates substituent effects in the ground state via a bond polarization mechanism.A comparison with available data for 4-substituted and 4,4'-disubstituted diphenylmethanes shows that the SiMe2 group is a better transmitter of electronic effects that the CH2 group. Keywords: Silicon; 29Si NMR; 13C NMR; Substituent effects; MO calculations

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