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(R)-8-Benzyloxy-6-hydroxy-7,7-dimethyl-oct-1-en-4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 909016-28-0 Structure
  • Basic information

    1. Product Name: (R)-8-Benzyloxy-6-hydroxy-7,7-dimethyl-oct-1-en-4-one
    2. Synonyms: (R)-8-Benzyloxy-6-hydroxy-7,7-dimethyl-oct-1-en-4-one
    3. CAS NO:909016-28-0
    4. Molecular Formula:
    5. Molecular Weight: 276.376
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 909016-28-0.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: (R)-8-Benzyloxy-6-hydroxy-7,7-dimethyl-oct-1-en-4-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-8-Benzyloxy-6-hydroxy-7,7-dimethyl-oct-1-en-4-one(909016-28-0)
    11. EPA Substance Registry System: (R)-8-Benzyloxy-6-hydroxy-7,7-dimethyl-oct-1-en-4-one(909016-28-0)
  • 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: 909016-28-0(Hazardous Substances Data)

909016-28-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 909016-28-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,9,0,1 and 6 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 909016-28:
(8*9)+(7*0)+(6*9)+(5*0)+(4*1)+(3*6)+(2*2)+(1*8)=160
160 % 10 = 0
So 909016-28-0 is a valid CAS Registry Number.

909016-28-0Downstream Products

909016-28-0Relevant articles and documents

Enantioselective synthesis of aurisides A and B, cytotoxic macrolide glycosides of marine origin

Suenaga, Kiyotake,Hoshino, Hiroshi,Yoshii, Takanori,Mori, Kazunori,Sone, Hiroki,Bessho, Yuhki,Sakakura, Akira,Hayakawa, Ichiro,Yamada, Kiyoyuki,Kigoshi, Hideo

, p. 7687 - 7698 (2007/10/03)

The enantioselective synthesis of aurisides A and B, macrolide glycosides of marine origin, was achieved by a convergent approach. The C1-C9 segment 4 was prepared from (R)-pantolactone, and the C10-C17 segment 14 was synthesized from (R)-glycidyl trityl

Synthesis of the aglycon of aurisides A and B, cytotoxic macrolide glycosides of marine origin

Sone, Hiroki,Suenaga, Kiyotake,Bessho, Yuhki,Kondo, Takashi,Kigoshi, Hideo,Yamada, Kiyoyuki

, p. 85 - 86 (2007/10/03)

The synthesis of the aglycon of aurisides A and B was achieved from (R)-pantolactone in 29 steps using the Nozaki reaction and the Yamaguchi macrolactonization as key steps.

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