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<2-dimethyl(phenoxy)silylethyl>diphenylphosphine oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 103676-01-3 Structure
  • Basic information

    1. Product Name: <2-dimethyl(phenoxy)silylethyl>diphenylphosphine oxide
    2. Synonyms: <2-dimethyl(phenoxy)silylethyl>diphenylphosphine oxide
    3. CAS NO:103676-01-3
    4. Molecular Formula:
    5. Molecular Weight: 380.499
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 103676-01-3.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: <2-dimethyl(phenoxy)silylethyl>diphenylphosphine oxide(CAS DataBase Reference)
    10. NIST Chemistry Reference: <2-dimethyl(phenoxy)silylethyl>diphenylphosphine oxide(103676-01-3)
    11. EPA Substance Registry System: <2-dimethyl(phenoxy)silylethyl>diphenylphosphine oxide(103676-01-3)
  • 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: 103676-01-3(Hazardous Substances Data)

103676-01-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103676-01-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,6,7 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 103676-01:
(8*1)+(7*0)+(6*3)+(5*6)+(4*7)+(3*6)+(2*0)+(1*1)=103
103 % 10 = 3
So 103676-01-3 is a valid CAS Registry Number.

103676-01-3Downstream Products

103676-01-3Relevant articles and documents

BIS(TRIMETHYLSILYL)PEROXIDE AS A VERSATILE REAGENT FOR SELECTIVE GENERATION OF OXYPHOSPHORYL GROUP

Wozniak, L.,Kowalski, J.,Chojnowski, J.

, p. 4965 - 4968 (1985)

Bis(trimethylsilyl)peroxide, Me3SiOOSiMe3, (BSPO) oxidizes phosphines and phosphites to respective oxyphosphoryl derivatives with retention of the configuration at the phosphorus atom.It also converts thiophosphoryl function to oxyphosphoryl function with inversion of the configuration at phosphorus.High yields and high stereoselectivities of these processes render them useful for the synthetic application.

The modification of reactivity at silicon centre by a remote phosphorus group

Kowalski, Jozef,Chojnowski, Julian

, p. 285 - 296 (2007/10/02)

The compounds X(CH2)nSiMe2(OPh) (X = H, n = 2, 3; X = PPh2, n = 1, 2, 3; X = P(O)Ph2, n = 2, 3; X = P(S)Ph2, n = 1, 2, 3) having silicon and phosphorus bridged by carbon chains, have been synthesized.The kinetics of acid- and basecatalysed solvolytic cleavage of phenoxyl group from these compounds in methanol have been investigated.The kinetic results obtained in the presence of bases can be interpreted in terms of polar and steric effects alone, but there was an unexpected enhancement of the reactivity in the case of the P=O-containing substrates in the acidic media.The solvent kinetic isotope effects are best interpreted in terms of participation by the P=O group as a base rather than as a nucleophile attacking the silicon centre.

SILYLPEROXIDES AS SELECTIVE OXYGENATION REAGENTS IN PHOSPHORUS CHEMISRTY

Kowalski, Jozef,Wozniak, Lucyna,Chojnowski, Julian

, p. 125 - 128 (2007/10/02)

Bis(trimethylsilyl)peroxide (BSPO) can be used for chemo- and stereoselective generation of P=O group by oxygenation of P(III) centre and transformation of P=S and P=Se groups.

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