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T-Butyl(Dichloromethyl)Dimethylsilane, also known as t-butyl(dimethylsilyl)dichloromethane, is an organosilicon compound characterized by the chemical formula C6H15Cl2Si. It is a colorless liquid that serves as a reagent in organic synthesis, especially in the creation of silicon-containing polymers and materials. T-Butyl(Dichloromethyl)Dimethylsilane's structure features a t-butyl group and two chlorine atoms attached to a silicon atom, which makes it a valuable building block for the synthesis of novel silicon-based compounds. Its silicon-containing structure endows it with potential applications in the production of specialty chemicals, pharmaceuticals, and materials with distinctive properties. However, due to its reactivity, T-Butyl(Dichloromethyl)Dimethylsilane should be handled with care to prevent hazardous chemical reactions.

138983-08-1

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138983-08-1 Usage

Uses

Used in Organic Synthesis:
T-Butyl(Dichloromethyl)Dimethylsilane is used as a reagent for the synthesis of silicon-containing polymers and materials, leveraging its unique chemical structure to create new compounds with potential applications in various industries.
Used in Specialty Chemicals Production:
In the specialty chemicals industry, T-Butyl(Dichloromethyl)Dimethylsilane is utilized as a building block for the development of unique silicon-based compounds, contributing to the creation of innovative products with specific properties tailored for specialized applications.
Used in Pharmaceutical Industry:
T-Butyl(Dichloromethyl)Dimethylsilane is employed in the pharmaceutical sector for the synthesis of silicon-containing drugs, potentially enhancing the properties of medications and contributing to the development of novel therapeutic agents.
Used in Material Science:
In material science, T-Butyl(Dichloromethyl)Dimethylsilane is used as a precursor for the development of materials with unique properties, such as improved thermal stability, chemical resistance, or specific mechanical characteristics, by incorporating silicon into their structure.

Check Digit Verification of cas no

The CAS Registry Mumber 138983-08-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,9,8 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 138983-08:
(8*1)+(7*3)+(6*8)+(5*9)+(4*8)+(3*3)+(2*0)+(1*8)=171
171 % 10 = 1
So 138983-08-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H16Cl2Si/c1-7(2,3)10(4,5)6(8)9/h6H,1-5H3

138983-08-1 Well-known Company Product Price

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  • Aldrich

  • (410683)  tert-Butyl(dichloromethyl)dimethylsilane  98%

  • 138983-08-1

  • 410683-1G

  • 884.52CNY

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138983-08-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl-(dichloromethyl)-dimethylsilane

1.2 Other means of identification

Product number -
Other names Dichlor<(1,1-dimethylethyl)dimethylsilyl>methan

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:138983-08-1 SDS

138983-08-1Relevant academic research and scientific papers

tert-Butyldimethylsilyldihalomethyllithium as a dihalomethylene dianion synthon. 1,3-Rearrangement and 1,4-rearrangement of silyl group from carbon to oxide

Shinokubo, Hiroshi,Miura, Katsukiyo,Oshima, Koichiro,Utimoto, Kiitiro

, p. 503 - 514 (2007/10/03)

One-pot synthesis of R1CH(OSiMe2-t-Bu)CX2CH(OH)R2 (X = Cl, Br) by successive addition of two different aldehydes (R1CHO and R2CHO) has been achieved starting from tert-butyldimethylsilyldihalomethyllithium. Treatment of a THF solution of the title carbanion (X = Cl) with p-MeOC6H4CHO or n-BuCHO followed by an addition of HMPA and benzaldehyde gave the corresponding 1,3-diol monosilyl ether in 83% or 45% yield, respectively. The use of oxirane in place of aldehyde as the first electrophile followed by addition of benzaldehyde provided 1,4-diol monosilyl ether.

tert-Butyldimethylsilyldichloromethyllithium as a dichloromethylene dianion synthon. 1,3-Rearrangement of silyl group from carbon to oxide

Shinokubo, Hiroshi,Miura, Katsukiyo,Oshima, Koichiro,Utimoto, Kiitiro

, p. 1951 - 1954 (2007/10/02)

One-pot synthesis of R1CH(OSiMe2-t-Bu)CCl2CH(OH)R2 by successive addition of two different electrophiles has been achieved starting.

Bis(methylene)phosphoranes - Synthesis, Spectroscopic Investigations and Thermal Isomerizations to λ3-Phosphiranes

Becker, Petra,Brombach, Heike,David, Gabriele,Leuer, Martina,Metternich, Hans-Juergen,Niecke, Edgar

, p. 771 - 782 (2007/10/02)

A great number of differently substituted bis(methylene)phosphoranes 10 2> are obtained by nucleophilic substitution from bis-chlorophosphorane (8).The reactions of dichlorophosphanes 1 and methylenephosphanes

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