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501419-03-0

3R-tert-butyldimethylsiloxy-2R-methyl-4-benzyloxy-1-iodobutane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 501419-03-0 Structure

  • Basic information

    1. Product Name: 3R-tert-butyldimethylsiloxy-2R-methyl-4-benzyloxy-1-iodobutane
    2. Synonyms: 3R-tert-butyldimethylsiloxy-2R-methyl-4-benzyloxy-1-iodobutane
    3. CAS NO:501419-03-0
    4. Molecular Formula:
    5. Molecular Weight: 434.433
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 501419-03-0.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: 3R-tert-butyldimethylsiloxy-2R-methyl-4-benzyloxy-1-iodobutane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3R-tert-butyldimethylsiloxy-2R-methyl-4-benzyloxy-1-iodobutane(501419-03-0)
    11. EPA Substance Registry System: 3R-tert-butyldimethylsiloxy-2R-methyl-4-benzyloxy-1-iodobutane(501419-03-0)

  • 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: 501419-03-0(Hazardous Substances Data)

501419-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 501419-03-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,4,1 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 501419-03:
(8*5)+(7*0)+(6*1)+(5*4)+(4*1)+(3*9)+(2*0)+(1*3)=100
100 % 10 = 0
So 501419-03-0 is a valid CAS Registry Number.

501419-03-0Relevant articles and documents

Enantioselective total synthesis of borrelidin

Duffey, Matthew O.,LeTiran, Arnaud,Morken, James P.

, p. 1458 - 1459 (2007/10/03)

The first total synthesis of the natural product borrelidin is described. The propionate fragment of the molecule was concisely synthesized through catalytic enantioselective reductive aldol reactions, a catalytic Negishi coupling, and a catalytic directed hydrogenation. The propionate segment was then fused to the vinyl iodide fragment through a catalytic Sonogashira coupling. Subsequent catalytic hydrostannylation and catalytic cyanation allowed access to the target structure. Copyright

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