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101047-40-9

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101047-40-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101047-40-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,0,4 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 101047-40:
(8*1)+(7*0)+(6*1)+(5*0)+(4*4)+(3*7)+(2*4)+(1*0)=59
59 % 10 = 9
So 101047-40-9 is a valid CAS Registry Number.

101047-40-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-trimethyl<2-(2-nitrophenyl)ethenyl>silane

1.2 Other means of identification

Product number -
Other names (E)-trimethyl[2-(2-nitrophenyl)ethenyl]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:101047-40-9 SDS

101047-40-9Downstream Products

101047-40-9Relevant articles and documents

PALLADIUM-CATALYSED ARYLATION OF VINYLTRIMETHYLSILANE IN THE PRESENCE OF SILVER NITRATE

Karabelas, Kostas,Hallberg, Anders

, p. 3131 - 3132 (1985)

A series of arylated vinyltrimethylsilanes have been prepared by means of Heck Arylation in the presence of silver nitrate, which serves to suppress the elimination of the silicon group and enhance the reaction rate.

Synthesis of (E)-(2-Arylethenyl)silanes by Palladium-Catalyzed Arylation of Vinylsilanes in the Presence of Silver Nitrate

Karabelas, Kostas,Hallberg, Anders

, p. 5286 - 5290 (2007/10/02)

A series of (E)-trimethyl(2-arylethenyl)silanes 1-16 and (E)-triethoxy(2-arylethenyl)silanes 17 and 18 has been synthesized by palladium-catalyzed arylation of the corresponding vinylsilanes, in the presence of silver nitrate.Apart from enhancing the rate of the reaction, silver nitrate also completely suppresses the desilylation.In the absence of silver salt, under ordinary Heck arylation conditions, styrene derivatives are formed in good yields.A possible mechanistic rationale for the formation of styrenes is discussed.

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