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CAS

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671184-49-9

Silane, tris(1-methylethyl)[(4,4,7-trimethyl-1,6-cycloheptadien-1-yl)oxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 671184-49-9 Structure

  • Basic information

    1. Product Name: Silane, tris(1-methylethyl)[(4,4,7-trimethyl-1,6-cycloheptadien-1-yl)oxy]-
    2. Synonyms:
    3. CAS NO:671184-49-9
    4. Molecular Formula: C19H36OSi
    5. Molecular Weight: 308.58
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 671184-49-9.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: Silane, tris(1-methylethyl)[(4,4,7-trimethyl-1,6-cycloheptadien-1-yl)oxy]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Silane, tris(1-methylethyl)[(4,4,7-trimethyl-1,6-cycloheptadien-1-yl)oxy]-(671184-49-9)
    11. EPA Substance Registry System: Silane, tris(1-methylethyl)[(4,4,7-trimethyl-1,6-cycloheptadien-1-yl)oxy]-(671184-49-9)

  • 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: 671184-49-9(Hazardous Substances Data)

671184-49-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 671184-49-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,1,1,8 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 671184-49:
(8*6)+(7*7)+(6*1)+(5*1)+(4*8)+(3*4)+(2*4)+(1*9)=169
169 % 10 = 9
So 671184-49-9 is a valid CAS Registry Number.

671184-49-9Downstream Products

671184-49-9Relevant articles and documents

Rapid Assembly of Polycyclic Substances by a Multicomponent Cascade (4 + 2)-(2 + 2) Cycloadditions: Total Synthesis of the Proposed Structure of Paesslerin A

Inanaga, Kazato,Takasu, Kiyosei,Ihara, Masataka

, p. 1352 - 1353 (2004)

A versatile method for stereoselective formation of multisubstituted bicyclo[4.2.0]octane framework has been developed by means of catalytic (4 + 2)-(2 + 2) cycloaddition reactions. Its application to the synthesis of a substance reported to be the cytotoxic sesquiterpene, paesslerin A, is described, and it has been made clear that a revision of the structure of natural paesslerin A is required. Copyright

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