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2-Propenal, 3-phenyl-2-[(trimethylsilyl)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89809-41-6

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89809-41-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89809-41-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,8,0 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 89809-41:
(7*8)+(6*9)+(5*8)+(4*0)+(3*9)+(2*4)+(1*1)=186
186 % 10 = 6
So 89809-41-6 is a valid CAS Registry Number.

89809-41-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenyl-2-(trimethylsilylmethyl)prop-2-enal

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:89809-41-6 SDS

89809-41-6Downstream Products

89809-41-6Relevant academic research and scientific papers

FUNCTIONAL ALLYLSILANES: REACTIVITY OF PYRROLIDINOALLYLSILANES TOWARDS ELECTROPHILES

Corriu, R.J.P.,Huynh, V.,Moreau, J.J.E.

, p. 283 - 294 (1983)

(3-Pyrrolidinoallyl)trimethylsilane (1) and (1-pyrrolidinoallyl)trimethylsilane (2) have been prepared from allylpyrrolidine.Compound 1 is both an allylsilane and an enamine.It exhibits enamine-type reactions with electrophiles leading to substituted β-tr

Synthesis of 3-silyl-2(5H)-furanone by rhodium-catalyzed cyclocarbonylation

Fukuta, Yukimasa,Matsuda, Isamu,Itoh, Kenji

, p. 1301 - 1304 (2001)

3-Silyl-2(5H)-furanones are readily formed by the rhodium-catalyzed cyclocarbonylation of propargyl alcohol derivatives bearing a trialkylsilyl group on the terminal sp-carbon under hydroformylation conditions. The following two requirements must be satisfied for the success of this protocol; (i) the presence of a silyl group on the sp-carbon, and (ii) the presence of a catalytic amount of Rh4(CO)12.

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