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CAS

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1017238-08-2

S-ethyl (3S,5S,7S)-7-{[tert-butyl(diphenyl)silyl]oxy}-5-methoxy-3-methyldecanethioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1017238-08-2 Structure

  • Basic information

    1. Product Name: S-ethyl (3S,5S,7S)-7-{[tert-butyl(diphenyl)silyl]oxy}-5-methoxy-3-methyldecanethioate
    2. Synonyms: S-ethyl (3S,5S,7S)-7-{[tert-butyl(diphenyl)silyl]oxy}-5-methoxy-3-methyldecanethioate
    3. CAS NO:1017238-08-2
    4. Molecular Formula:
    5. Molecular Weight: 514.845
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1017238-08-2.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: S-ethyl (3S,5S,7S)-7-{[tert-butyl(diphenyl)silyl]oxy}-5-methoxy-3-methyldecanethioate(CAS DataBase Reference)
    10. NIST Chemistry Reference: S-ethyl (3S,5S,7S)-7-{[tert-butyl(diphenyl)silyl]oxy}-5-methoxy-3-methyldecanethioate(1017238-08-2)
    11. EPA Substance Registry System: S-ethyl (3S,5S,7S)-7-{[tert-butyl(diphenyl)silyl]oxy}-5-methoxy-3-methyldecanethioate(1017238-08-2)

  • 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: 1017238-08-2(Hazardous Substances Data)

1017238-08-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1017238-08-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,7,2,3 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1017238-08:
(9*1)+(8*0)+(7*1)+(6*7)+(5*2)+(4*3)+(3*8)+(2*0)+(1*8)=112
112 % 10 = 2
So 1017238-08-2 is a valid CAS Registry Number.

1017238-08-2Relevant articles and documents

Formal total synthesis of neopeltolide

Vintonyak, Viktor V.,Maier, Martin E.

supporting information; experimental part, p. 1239 - 1242 (2009/04/12)

A concise synthesis of the core structure of the macrolide neopeltolide was develop featuring a Prins cyclization to fashion the pyran ring. Key steps in the synthesis of aldehyde 16 were a Leiqhton allylation and a Feringa-Minnaard asymmetric methyl cuprate addition to an unsaturated thioester. For lactonization, a classical Yamaguchin macrolactonization was used. The longest linear sequence consists of 17 steps providing lactone 26 with an overall yield of 23%.

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