2943-70-6 Usage
Uses
Used in Chemical Synthesis:
1,3-BIS(DICHLOROMETHYL)-1,1,3,3-TETRAMETHYLDISILOXANE is used as a solvent and intermediate in chemical synthesis for its ability to facilitate reactions and produce desired organic compounds.
Used in Silicone Production:
In the Silicone Industry, 1,3-BIS(DICHLOROMETHYL)-1,1,3,3-TETRAMETHYLDISILOXANE is used as a precursor in the production of silicone-based polymers, which are known for their versatility and wide range of applications, including sealants, adhesives, and elastomers.
Used in Adhesive Manufacturing:
1,3-BIS(DICHLOROMETHYL)-1,1,3,3-TETRAMETHYLDISILOXANE is used as a component in the manufacturing of adhesives, where its properties contribute to the formulation of strong, durable, and flexible bonding agents.
Used in Industrial Product Manufacturing:
1,3-BIS(DICHLOROMETHYL)-1,1,3,3-TETRAMETHYLDISILOXANE is utilized in various industrial applications, where it serves as a key ingredient in the production of a range of products, highlighting its importance in the manufacturing sector.
Check Digit Verification of cas no
The CAS Registry Mumber 2943-70-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,4 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2943-70:
(6*2)+(5*9)+(4*4)+(3*3)+(2*7)+(1*0)=96
96 % 10 = 6
So 2943-70-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H14Cl4OSi2/c1-12(2,5(7)8)11-13(3,4)6(9)10/h5-6H,1-4H3
2943-70-6Relevant academic research and scientific papers
Selectivite de la scission Si-C dans des composes du type Me3SiCH2Σ; une synthese originale et sure de l'iodoacetate d'ethyle
Bordeau, M.,Djamei, S. M.,Dunogues, J.
, p. 413 - 417 (2007/10/02)
The regiochemistry of the electrophilic cleavage of the SiCsp3 bond in compounds Me3SiCH2Σ (Σ = Me, Pr, Cl, COOEt) and Me3SiCHΣ2 (Σ = Cl) has been investigated using ICl, Me3SiOSO2Cl and HO3SCl as the electrophiles.When Σ = Pr or Cl a regioselective cleavage of the Si-CH3 bond was observed, producing silylated chlorosulfonates or sulfates which often were new compounds.With Σ = COOEt a regiospecific splitting of the Si-CH2COOEt bond was observed.This confirms the synthetic potential of ethyl trimethylsilylacetate.
