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CAS

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590362-03-1

Benzenemethanol, a-[3-methyl-2-(1-methylethenyl)-2-butenyl]-2-[[[tris(1-methylethyl)silyl]oxy ]methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 590362-03-1 Structure

  • Basic information

    1. Product Name: Benzenemethanol, a-[3-methyl-2-(1-methylethenyl)-2-butenyl]-2-[[[tris(1-methylethyl)silyl]oxy ]methyl]-
    2. Synonyms:
    3. CAS NO:590362-03-1
    4. Molecular Formula: C25H42O2Si
    5. Molecular Weight: 402.693
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 590362-03-1.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: Benzenemethanol, a-[3-methyl-2-(1-methylethenyl)-2-butenyl]-2-[[[tris(1-methylethyl)silyl]oxy ]methyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenemethanol, a-[3-methyl-2-(1-methylethenyl)-2-butenyl]-2-[[[tris(1-methylethyl)silyl]oxy ]methyl]-(590362-03-1)
    11. EPA Substance Registry System: Benzenemethanol, a-[3-methyl-2-(1-methylethenyl)-2-butenyl]-2-[[[tris(1-methylethyl)silyl]oxy ]methyl]-(590362-03-1)

  • 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: 590362-03-1(Hazardous Substances Data)

590362-03-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 590362-03-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,9,0,3,6 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 590362-03:
(8*5)+(7*9)+(6*0)+(5*3)+(4*6)+(3*2)+(2*0)+(1*3)=151
151 % 10 = 1
So 590362-03-1 is a valid CAS Registry Number.

590362-03-1Relevant articles and documents

A stereoselective intramolecular Diels-Alder strategy for the tricyclo[9.3.1.03,8]pentadecane core of aromatic C-ring taxanes

Smil, David V.,Laurent, Alain,Spassova, Nidejda S.,Fallis, Alex G.

, p. 5129 - 5132 (2003)

A stereoselective Lewis acid-catalyzed and chelation controlled intramolecular Diels-Alder entry into the tricyclo[9.3.1.03,8]pentadecane core of aromatic C-ring taxanes is described. The approach affords an efficient, high yield, access to aromatic C-ring taxanes variably functionalized at the C2, C4, C5, and C9 positions.

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