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(4S,6R)-4-Allyl-6-(2-benzyloxy-1,1-dimethyl-ethyl)-2,2-dimethyl-[1,3]dioxane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 202406-58-4 Structure
  • Basic information

    1. Product Name: (4S,6R)-4-Allyl-6-(2-benzyloxy-1,1-dimethyl-ethyl)-2,2-dimethyl-[1,3]dioxane
    2. Synonyms: (4S,6R)-4-Allyl-6-(2-benzyloxy-1,1-dimethyl-ethyl)-2,2-dimethyl-[1,3]dioxane
    3. CAS NO:202406-58-4
    4. Molecular Formula:
    5. Molecular Weight: 318.456
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 202406-58-4.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: (4S,6R)-4-Allyl-6-(2-benzyloxy-1,1-dimethyl-ethyl)-2,2-dimethyl-[1,3]dioxane(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4S,6R)-4-Allyl-6-(2-benzyloxy-1,1-dimethyl-ethyl)-2,2-dimethyl-[1,3]dioxane(202406-58-4)
    11. EPA Substance Registry System: (4S,6R)-4-Allyl-6-(2-benzyloxy-1,1-dimethyl-ethyl)-2,2-dimethyl-[1,3]dioxane(202406-58-4)
  • 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: 202406-58-4(Hazardous Substances Data)

202406-58-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 202406-58-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,2,4,0 and 6 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 202406-58:
(8*2)+(7*0)+(6*2)+(5*4)+(4*0)+(3*6)+(2*5)+(1*8)=84
84 % 10 = 4
So 202406-58-4 is a valid CAS Registry Number.

202406-58-4Downstream Products

202406-58-4Relevant 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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