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18056-97-8

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18056-97-8 Usage

Uses

suzuki reaction

Check Digit Verification of cas no

The CAS Registry Mumber 18056-97-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,0,5 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 18056-97:
(7*1)+(6*8)+(5*0)+(4*5)+(3*6)+(2*9)+(1*7)=118
118 % 10 = 8
So 18056-97-8 is a valid CAS Registry Number.

18056-97-8SDS

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 triethoxy-(4-phenylphenyl)silane

1.2 Other means of identification

Product number -
Other names 4-triethoxysilyl-1,1'-biphenyl

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:18056-97-8 SDS

18056-97-8Relevant articles and documents

Rhodium(III)-Catalyzed Direct C-H Arylation of Various Acyclic Enamides with Arylsilanes

Li, Xiaolan,Sun, Kai,Shen, Wenjuan,Zhang, Yong,Lu, Ming-Zhu,Luo, Xuzhong,Luo, Haiqing

supporting information, p. 31 - 36 (2021/01/09)

The stereoselective β-C(sp2)-H arylation of various acyclic enamides with arylsilanes via Rh(III)-catalyzed cross-coupling reaction was illustrated. The methodology was characterized by extraordinary efficacy and stereoselectivity, a wide scope of substrates, good functional group tolerance, and the adoption of environmentally friendly arylsilanes. The utility of this present method was evidenced by the gram-scale synthesis and further elaboration of the product. In addition, Rh(III)-catalyzed C-H activation is considered to be the critical step in the reaction mechanism.

Silver-mediated fluorination of aryl silanes

Tang, Pingping,Ritter, Tobias

supporting information; experimental part, p. 4449 - 4454 (2011/08/03)

A regiospecific silver-mediated fluorination of aryl silanes is reported. The reaction is operationally simple, and employs Ag2O as readily available, inexpensive silver source, which can be recovered.

Selective hydrosilylation method using hydrido (hydrocarbonoxy) silane

-

, (2008/06/13)

A method for hydrosilylating a vinyl-substituted aromatic compound comprising reacting a hydrido (hydrocarbonoxy)silane compound with the vinyl-substituted aromatic compound in the presence of a platinum or platinum compound catalyst and a carboxylic acid

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