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93782-13-9

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93782-13-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93782-13-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,7,8 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 93782-13:
(7*9)+(6*3)+(5*7)+(4*8)+(3*2)+(2*1)+(1*3)=159
159 % 10 = 9
So 93782-13-9 is a valid CAS Registry Number.

93782-13-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-(2,2-dibromoethenyl)phenoxy]-trimethylsilane

1.2 Other means of identification

Product number -
Other names -

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:93782-13-9 SDS

93782-13-9Relevant articles and documents

Gas-Phase Thermal Rearrangements of Potential Vinylidene Precursors to Silylbenzofurans and Silylbenzopyrans

Barton, Thomas J.,Groh, Brian L.

, p. 158 - 166 (2007/10/02)

In an attempt to utilize the considerable migratory aptitude of silicon in the synthesis of 3-silylbenzofurans, the flash vacuum pyrolysis (FVP) of o-phenol was found to provide not only the furan expected from vinylidene cyclization but two isomers resulting from initial 1,5-hydrogen migration from oxygen to form an intermediate allenyl ketone.FVP of 2-(trimethylsilyl)4,5-dihydrofuran produced an unprecedented gas-phase reductive elimination to a vinylidene. o-Ethynyl- and o-propynylanisoles did not afford benzopyrans through vinylidene/C-H(Me) insertion but underwent radical transformations.However, o-anisole unexpectedly extruded Me2Si to form 2-ethylbenzofuran as the only product.Various mechanisms for this remarkable decomposition are considered.The acyclic analogue 1-(trimethylsilyl)-4-methoxybut-1-yn-3-ene pyrolytically extruded not Me2Si but carbon monoxide! This is rationalized as proceeding through an initial 1,5-methyl migration from oxygen to carbon.

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