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(t-Butyldimethylsilyl)allene is a chemical compound that features a (t-butyldimethylsilyl) group attached to an allene molecule, playing a significant role in organic synthesis as a versatile building block for constructing more complex molecules.

176545-76-9

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176545-76-9 Usage

Uses

Used in Organic Synthesis:
(t-Butyldimethylsilyl)allene is used as a building block for creating complex organic molecules due to its unique structure and reactivity. The (t-butyldimethylsilyl) group acts as a protecting group that can be removed under specific conditions, revealing a functional group for further chemical reactions. This property is highly valuable in the synthesis of various organic compounds.
Used in Cycloadditions:
In the field of organic chemistry, (t-Butyldimethylsilyl)allene is used as a reactive center for cycloadditions, a type of chemical reaction where two or more unsaturated molecules (often organic) combine to form a cyclic compound. This application is crucial for the development of novel cyclic compounds with potential applications in various industries.
Used in Cross-Coupling Reactions:
(t-Butyldimethylsilyl)allene is also utilized in cross-coupling reactions, which are essential for the formation of carbon-carbon bonds in organic chemistry. These reactions are widely used in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials.
Used in Polymerization Processes:
Furthermore, (t-Butyldimethylsilyl)allene is employed in polymerization processes to create polymers with specific properties. The allene moiety's reactivity allows for the development of novel polymers with potential applications in materials science, such as in the production of plastics, elastomers, and other polymer-based products.
Used in the Pharmaceutical Industry:
(t-Butyldimethylsilyl)allene is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its ability to participate in a wide range of chemical reactions makes it a valuable tool for the development of new drugs and therapeutic agents.
Used in the Materials Science Industry:
In materials science, (t-Butyldimethylsilyl)allene is used for the development of advanced materials with specific properties, such as improved strength, flexibility, or chemical resistance. These materials can be utilized in various applications, including aerospace, automotive, and electronics industries.

Check Digit Verification of cas no

The CAS Registry Mumber 176545-76-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,5,4 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 176545-76:
(8*1)+(7*7)+(6*6)+(5*5)+(4*4)+(3*5)+(2*7)+(1*6)=169
169 % 10 = 9
So 176545-76-9 is a valid CAS Registry Number.

176545-76-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl-dimethyl-propa-1,2-dienylsilane

1.2 Other means of identification

Product number -
Other names tertbutyldimethylsilylpropa-1,2-diene

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:176545-76-9 SDS

176545-76-9Downstream Products

176545-76-9Relevant academic research and scientific papers

Regioselective allene synthesis and propargylations with propargyl diethanolamine boronates

Fandrick, Daniel R.,Reeves, Jonathan T.,Tan, Zhulin,Lee, Heewon,Song, Jinhua J.,Yee, Nathan K.,Senanayake, Chris H.

supporting information; experimental part, p. 5458 - 5461 (2010/03/01)

"Chemical Equation Presented" The utility of propargyl diethanolamine boronates as reagents for the preparation of allenes and homopropargylic alcohols is presented. Protonolysis with TFA and electrophilic substitution with N-halosuccinimides proceeded wi

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