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Silane, (2,5-dimethylphenyl)dimethylphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

135609-07-3

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135609-07-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135609-07-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,6,0 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 135609-07:
(8*1)+(7*3)+(6*5)+(5*6)+(4*0)+(3*9)+(2*0)+(1*7)=123
123 % 10 = 3
So 135609-07-3 is a valid CAS Registry Number.

135609-07-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,5-dimethylphenyl)-dimethyl-phenylsilane

1.2 Other means of identification

Product number -
Other names Dimethyl-(2,5-dimethyldiphenyl)phenylsilane

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:135609-07-3 SDS

135609-07-3Relevant academic research and scientific papers

Site-Selective Silylation of Arenes Mediated by Thianthrene S-Oxide

Wu, Yichen,Huang, Yu-Hao,Chen, Xiao-Yue,Wang, Peng

supporting information, p. 6657 - 6661 (2020/09/02)

The thianthrene S-oxide (TTSO)-mediated site-selective silylation of arenes has been realized via a thianthrenation/Pd-catalyzed silylation sequence. This method features a broad substrate scope and wide functional group tolerance under mild conditions and allows the synthesis of a set of (hetero)arylsilanes with operationally simple manipulations. The application and generality of the approach were further demonstrated by the late-stage functionalization of marketed drugs. This reaction also represents the first example of a Pd-catalyzed silylation reaction of aryl sulfonium salts.

Catalytic reduction of aryl trialkylammonium salts to aryl silanes and arenes

Rand, Alexander W.,Montgomery, John

, p. 5338 - 5344 (2019/05/29)

A new approach for the reduction of aryl ammonium salts to arenes or aryl silanes using nickel catalysis is reported. This method displays excellent ligand-controlled selectivity based on the N-heterocyclic carbene (NHC) ligand employed. Utilizing a large NHC in non-polar solvents generates aryl silanes, while small NHCs in polar solvents promote reduction to arenes. Several classes of aryl silanes can be accessed from simple aniline building blocks, including those useful for cross-couplings, oxidations, and halogenations. The reaction conditions are mild, functional group tolerant, and provide efficient access to a variety of benzene derivatives.

Novel cyclohexylsilyl- or phenylsilyl-substituted poly(p-phenylene vinylene)s via the halogen precursor route and Gilch polymerization

Ahn, Taek,Ko, Seung-Won,Lee, Jaemin,Shim, Hong-Ku

, p. 3495 - 3505 (2007/10/03)

Novel cyclohexylsilyl- or phenylsilyl-substituted poly(1,4-phenylene vinylene) (PPV) derivatives, poly[2,5-bis(dimethylcyclohexylsilyl)-1,4-phenylene vinylene] (BDMCyS-PPV), poly[2,5-bis(dimethylphenylsilyl)-1,4-phenylene vinylene] (BDMPS-PPV), poly[2-dim

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