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Disilanamine, 2,2'-(1,4-phenylene)bis[N,N-diethyl-1,1-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 558472-83-6 Structure
  • Basic information

    1. Product Name: Disilanamine, 2,2'-(1,4-phenylene)bis[N,N-diethyl-1,1-diphenyl-
    2. Synonyms:
    3. CAS NO:558472-83-6
    4. Molecular Formula: C38H48N2Si4
    5. Molecular Weight: 645.155
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 558472-83-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Disilanamine, 2,2'-(1,4-phenylene)bis[N,N-diethyl-1,1-diphenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Disilanamine, 2,2'-(1,4-phenylene)bis[N,N-diethyl-1,1-diphenyl-(558472-83-6)
    11. EPA Substance Registry System: Disilanamine, 2,2'-(1,4-phenylene)bis[N,N-diethyl-1,1-diphenyl-(558472-83-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 558472-83-6(Hazardous Substances Data)

558472-83-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 558472-83-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,8,4,7 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 558472-83:
(8*5)+(7*5)+(6*8)+(5*4)+(4*7)+(3*2)+(2*8)+(1*3)=196
196 % 10 = 6
So 558472-83-6 is a valid CAS Registry Number.

558472-83-6Downstream Products

558472-83-6Relevant articles and documents

Tailor-made synthesis of functional substituted oligo- and polysilanes from silyl triflates and (aminosilyl)lithium compounds

Uhlig, Wolfram

, p. 70 - 78 (2003)

Diethylamino substituted silyllithium compounds have been prepared in situ from the corresponding phenylchlorosilanes and lithium. These reagents undergo coupling reactions with triflate derivatives of silanes and oligosilanes. Exchange processes analogous to metal-halogen exchange and Si-Si bond cleavage, which are side reactions with chlorosilanes, were not observed. Based on the coupling reaction and the amino-to-triflate transformation, functionalized tri-, tetra-, penta- and hexasilanes have been synthesized. α,ω-Triflate substituted oligosilanes containing π-systems have also been obtained. These compounds are useful building blocks for new organosilicon polymers. The formation of the silicon polymers at low temperatures, in short reaction times, and with high yields is reported. The 29Si-NMR spectra indicate a regular, alternating arrangement of the building blocks in the polymer backbone.

Tailor-made synthesis of functional substituted oligosilanes from silyl triflates and (aminosilyl)lithium compounds

Uhlig, Wolfram

, p. 183 - 190 (2007/10/03)

Diethylamino substituted silyllithium compounds have been prepared in situ from the corresponding phenylchlorosilanes and lithium. These reagents undergo coupling reactions with triflate derivatives of silanes and oligosilanes. Exchange processes analogou

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