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2,2-diethoxy-1-(trimethylsilyl)-1-aza-2-silacyclopentane is a chemical compound with the formula C9H23NO2Si. It is a silacyclopentane derivative characterized by the presence of two ethoxy groups and a trimethylsilyl group attached to the silicon atom. 2,2-diethoxy-1-(trimethylsilyl)-1-aza-2-silacyclopentane is recognized for its unique structure and reactivity, making it a valuable building block in organosilicon chemistry for the synthesis of a variety of silicon-containing compounds.

21297-72-3

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21297-72-3 Usage

Uses

Used in Organosilicon Chemistry:
2,2-diethoxy-1-(trimethylsilyl)-1-aza-2-silacyclopentane is used as a versatile building block for the synthesis of various silicon-containing compounds. Its unique structure allows for the creation of complex molecules with potential applications across different fields.
Used in Materials Science:
In the field of materials science, 2,2-diethoxy-1-(trimethylsilyl)-1-aza-2-silacyclopentane is utilized for its potential to contribute to the development of new materials with enhanced properties, such as improved thermal stability or specific optical characteristics, due to its silicon-containing nature.
Used in Pharmaceutical Industry:
2,2-diethoxy-1-(trimethylsilyl)-1-aza-2-silacyclopentane is employed as a key intermediate in the synthesis of pharmaceuticals. Its reactivity and structural features enable the production of silicon-containing drug molecules that may exhibit novel therapeutic properties or improved pharmacokinetics.
Used in Agrochemicals:
2,2-diethoxy-1-(trimethylsilyl)-1-aza-2-silacyclopentane is also used in agrochemicals, where its silicon-containing structure can be leveraged to develop new pesticides or fertilizers with enhanced efficacy and reduced environmental impact.
Overall, 2,2-diethoxy-1-(trimethylsilyl)-1-aza-2-silacyclopentane's diverse applications stem from its unique structural attributes and reactivity, positioning it as an important compound in the advancement of various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 21297-72-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,2,9 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 21297-72:
(7*2)+(6*1)+(5*2)+(4*9)+(3*7)+(2*7)+(1*2)=103
103 % 10 = 3
So 21297-72-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H25NO2Si2/c1-6-12-15(13-7-2)10-8-9-11(15)14(3,4)5/h6-10H2,1-5H3

21297-72-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-diethoxy-1-trimethylsilanyl-[1,2]azasilolidine

1.2 Other means of identification

Product number -
Other names 2,2-DIETHOXY-1-(TRIMETHYLSILYL)-1,2-AZASILOLIDINE

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:21297-72-3 SDS

21297-72-3Downstream Products

21297-72-3Relevant academic research and scientific papers

METHOD FOR PRODUCING N-SILYLAMINOALKYLSILANE COMPOUND

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Paragraph 0059-0060; 0063-0065; 0076-0077, (2019/08/02)

Shown is a method for producing an N-silylaminoalkylsilane compound. The N-silylaminoalkylsilane compound is produced by allowing an aminoalkylsilane compound to react with a monochlorosilane compound in the presence of a tertiary amine compound having an

Formation of 1-aza-2-silacyclopentanes and unexpected products from the insertion of phenylisocyanate into 2,2-dimethyl-1-(trimethylsilyl)-1-aza-2-silacyclopentane

Herbig, Marcus,B?hme, Uwe,Schwarzer, Anke,Kroke, Edwin

, p. 11 - 19 (2018/05/04)

Substances like 3-aminopropyltriethoxysilane are often used as adhesive promoters in various formulations for coatings or to adjust the properties of siloxanes and other polymers. Cyclisation of similar substances is also interesting because of the formation of the Si-N bond. 1-Aza-2-silacyclopentanes were synthesised from 3-aminopropylalkoxysilanes by intramolecular condensation reactions and substitution reactions at the silicon atom. The products tend to undergo ring-opening polymerisation. In contrast to literature reports, they can only be isolated as N-substituted derivatives. Phenylisocyanate inserts into the Si-N bonds of cyclic aminosilanes to form seven-membered heterocycles. Furthermore, phenylisocyanate reacts with N-H bonds in the same molecule. Two insertion products were isolated, and their crystal structures were determined.

Non-corrosive silicone RTV compositions

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, (2008/06/13)

Stable, substantially acid-free, one package, moisture curable RTV compositions are provided having a scavenger for chemically combined hydroxy groups of the formula STR1 where x equals 1 or 2 and y equals 0 to 3 inclusive. A method for providing the aforesaid moisture curable RTV compositions is also provided. Novel compounds of the formula STR2 where x equals 1 or 2 and y equals 0 to 2 inclusive are provided as are methods for making such novel compounds.

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