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CAS

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1261246-04-1

(2-ethylphenyl)diphenylsilane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1261246-04-1 Structure

  • Basic information

    1. Product Name: (2-ethylphenyl)diphenylsilane
    2. Synonyms: (2-ethylphenyl)diphenylsilane
    3. CAS NO:1261246-04-1
    4. Molecular Formula:
    5. Molecular Weight: 288.464
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1261246-04-1.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-ethylphenyl)diphenylsilane(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2-ethylphenyl)diphenylsilane(1261246-04-1)
    11. EPA Substance Registry System: (2-ethylphenyl)diphenylsilane(1261246-04-1)

  • 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: 1261246-04-1(Hazardous Substances Data)

1261246-04-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1261246-04-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,1,2,4 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1261246-04:
(9*1)+(8*2)+(7*6)+(6*1)+(5*2)+(4*4)+(3*6)+(2*0)+(1*4)=121
121 % 10 = 1
So 1261246-04-1 is a valid CAS Registry Number.

1261246-04-1Relevant articles and documents

Acceleration effects of phosphine ligands on the rhodium-catalyzed dehydrogenative silylation and germylation of unactivated C(sp3)-H bonds

Murai, Masahito,Takeshima, Hirotaka,Morita, Haruka,Kuninobu, Yoichiro,Takai, Kazuhiko

, p. 5407 - 5414 (2015)

The current work describes the marked rate of acceleration caused by phosphine ligands on the rhodium-catalyzed dehydrogenative silylation and germylation of unactivated C(sp3)-H bonds. The reactivity was affected by the steric and electronic n

Rhodium-catalyzed intramolecular silylation of unactivated C(sp 3)-H bonds

Kuninobu, Yoichiro,Nakahara, Takahiro,Takeshima, Hirotaka,Takai, Kazuhiko

supporting information, p. 426 - 428 (2013/03/13)

The treatment of a variety of hydrosilanes, each incorporating a benzylic C(sp3)-H bond, with a rhodium catalyst resulted in intramolecular dehydrogenative silylation. This silylation reaction was found to occur at typically unreactive C(sp3)-H bonds located at terminal positions on alkyl chains. Interestingly, the rhodium catalyst also promoted regioselective silylation at a site internal to an alkyl chain.

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