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491608-02-7

1-(2-bromo-3-methoxymethoxyphenyl)-6-(tert-butyldimethylsilanyloxy)hexan-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 491608-02-7 Structure

  • Basic information

    1. Product Name: 1-(2-bromo-3-methoxymethoxyphenyl)-6-(tert-butyldimethylsilanyloxy)hexan-1-ol
    2. Synonyms: 1-(2-bromo-3-methoxymethoxyphenyl)-6-(tert-butyldimethylsilanyloxy)hexan-1-ol
    3. CAS NO:491608-02-7
    4. Molecular Formula:
    5. Molecular Weight: 447.485
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 491608-02-7.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: 1-(2-bromo-3-methoxymethoxyphenyl)-6-(tert-butyldimethylsilanyloxy)hexan-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(2-bromo-3-methoxymethoxyphenyl)-6-(tert-butyldimethylsilanyloxy)hexan-1-ol(491608-02-7)
    11. EPA Substance Registry System: 1-(2-bromo-3-methoxymethoxyphenyl)-6-(tert-butyldimethylsilanyloxy)hexan-1-ol(491608-02-7)

  • 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: 491608-02-7(Hazardous Substances Data)

491608-02-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 491608-02-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,1,6,0 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 491608-02:
(8*4)+(7*9)+(6*1)+(5*6)+(4*0)+(3*8)+(2*0)+(1*2)=157
157 % 10 = 7
So 491608-02-7 is a valid CAS Registry Number.

491608-02-7Relevant articles and documents

Studies toward the total synthesis of mumbaistatin, a highly potent glucose-6-phosphate translocase inhibitor. Synthesis of a mumbaistatin analogue

Kaiser, Florian,Schwink, Lothar,Velder, Janna,Schmalz, Hans-Guenther

, p. 9248 - 9256 (2007/10/03)

A strategy for the total synthesis of the highly potent glucose-6-phosphate translocase inhibitor mumbaistatin (1) and structural analogues was elaborated. Such compounds represent a lead structure in the development of potential new drugs for the treatment of diabetes. To evaluate the general strategy, the close mumbaistatin analogue 10 was synthesized in a convergent manner. The anthraquinone building block 20 was efficiently prepared via aryne/phthalide annulation. After conversion of 20 into the corresponding 9,10-dimethoxyanthracene-1-carbaldehyde derivative (13), coupling with a lithiated arene (12) and subsequent multiple oxidation under Jones conditions yielded the mumbaistatin analogue 10. The preparation of the functionalized arene intermediates was achieved exploiting highly regioselective bromination and ortho-lithiation reactions.

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