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Silane, (1,1-dimethylethyl)[[(2E)-3-methyl-2,4-pentadienyl]oxy]diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

645386-38-5

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645386-38-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 645386-38-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,5,3,8 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 645386-38:
(8*6)+(7*4)+(6*5)+(5*3)+(4*8)+(3*6)+(2*3)+(1*8)=185
185 % 10 = 5
So 645386-38-5 is a valid CAS Registry Number.

645386-38-5SDS

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 tert-butyl-(3-methylpenta-2,4-dienoxy)-diphenylsilane

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:645386-38-5 SDS

645386-38-5Downstream Products

645386-38-5Relevant academic research and scientific papers

Highly convergent, stereospecific synthesis of 11-cis-retinoids by metal-catalyzed cross-coupling reactions of (Z)-1-alkenylmetals

Lopez, Susana,Montenegro, Javier,Saa, Carlos

, p. 9572 - 9581 (2008/04/05)

(Chemical Equation Presented) A stereospecific synthesis of 11-cis-retinoids has as its key step the hitherto unexplored palladium-catalyzed cross-coupling of trans-tnenyl electrophiles and (1Z,3E)-penta-1,3-dienyl boronates (a Suzuki-Miyaura reaction) or

Intramolecular Formal oxa-[3 + 3] Cycloaddition Approach to the ABD System of Phomactin A

Cole, Kevin P.,Hsung, Richard P.

, p. 4843 - 4846 (2007/10/03)

(Equation Presented) The ABD-ring of phomactin A was synthesized using an intramolecular formal oxa-[3 + 3] cycloaddion of an α,β-unsaturated iminium salt tethered to a 1,3-diketone. This represents the first time that the 12-membered ring has been formed

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