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CAS

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261617-85-0

(2R,5R,6R,9R)-1-benzyloxy-2,5;6,9-diepoxy-10-tetracosanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 261617-85-0 Structure

  • Basic information

    1. Product Name: (2R,5R,6R,9R)-1-benzyloxy-2,5;6,9-diepoxy-10-tetracosanone
    2. Synonyms:
    3. CAS NO:261617-85-0
    4. Molecular Formula:
    5. Molecular Weight: 486.736
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 261617-85-0.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: (2R,5R,6R,9R)-1-benzyloxy-2,5;6,9-diepoxy-10-tetracosanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2R,5R,6R,9R)-1-benzyloxy-2,5;6,9-diepoxy-10-tetracosanone(261617-85-0)
    11. EPA Substance Registry System: (2R,5R,6R,9R)-1-benzyloxy-2,5;6,9-diepoxy-10-tetracosanone(261617-85-0)

  • 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: 261617-85-0(Hazardous Substances Data)

261617-85-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 261617-85-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,1,6,1 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 261617-85:
(8*2)+(7*6)+(6*1)+(5*6)+(4*1)+(3*7)+(2*8)+(1*5)=140
140 % 10 = 0
So 261617-85-0 is a valid CAS Registry Number.

261617-85-0Upstream product

261617-85-0Relevant articles and documents

A facile route to bulladecin-type acetogenins - Total synthesis of asimilobin and correction of the configuration of its tetrahydrofuran segment

Wang, Zhi-Min,Tian, Shi-Kai,Shi, Min

, p. 349 - 356 (2000)

The most efficient method for the synthesis of the trans/threo/trans- bis(tetrahydrofuran) (THF) ring unit was established, and the first total synthesis of (-)-asimilobin and its diastereomer was then accomplished in twelve and fourteen steps, respectively, from trans-1,5,9-decatriene, by a convergent route with a Wittig reaction as the key step. By virtue of these synthetic results, the absolute configuration of the bis(THF) unit in naturally occurring asimilobin should be corrected.

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