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118298-83-2

Trimethyl-(1-phenyl-3,4-dihydro-naphthalen-2-yl)-silane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 118298-83-2 Structure

  • Basic information

    1. Product Name: Trimethyl-(1-phenyl-3,4-dihydro-naphthalen-2-yl)-silane
    2. Synonyms:
    3. CAS NO:118298-83-2
    4. Molecular Formula:
    5. Molecular Weight: 278.469
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 118298-83-2.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: Trimethyl-(1-phenyl-3,4-dihydro-naphthalen-2-yl)-silane(CAS DataBase Reference)
    10. NIST Chemistry Reference: Trimethyl-(1-phenyl-3,4-dihydro-naphthalen-2-yl)-silane(118298-83-2)
    11. EPA Substance Registry System: Trimethyl-(1-phenyl-3,4-dihydro-naphthalen-2-yl)-silane(118298-83-2)

  • 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: 118298-83-2(Hazardous Substances Data)

118298-83-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 118298-83-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,2,9 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 118298-83:
(8*1)+(7*1)+(6*8)+(5*2)+(4*9)+(3*8)+(2*8)+(1*3)=152
152 % 10 = 2
So 118298-83-2 is a valid CAS Registry Number.

118298-83-2Downstream Products

118298-83-2Relevant articles and documents

Synthesis of Vinyl Silanes from Vinyl Silane Phosphates

Koerwitz, Frederick L.,Hammond, Gerald B.,Wiemer, David F.

, p. 743 - 747 (2007/10/02)

To develop a new synthesis of vinyl silanes, a representative set of vinyl silane phosphates (VSP's) has been treated with several organocuprate reagents.With acyclic VSP's, phosphate substitution proceeds in generally good yields, giving a single stereoisomer of the vinyl silane with retention of the VSP stereochemistry.In the cyclic systems examined, yields are generally somewhat lower under the same reactions conditions.However, this new sequence offers a regiochemistry complementary to other syntheses of cyclic vinyl silanes, and an approach to higly substituted vinyl silanes applicable to both cyclic and acyclic systems.

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