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CAS

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358972-70-0

(3R,4S,5R,6R)-6-(N-benzylamino)-3,4,5-tris(benzyloxy)-1,8-nonadiene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 358972-70-0 Structure

  • Basic information

    1. Product Name: (3R,4S,5R,6R)-6-(N-benzylamino)-3,4,5-tris(benzyloxy)-1,8-nonadiene
    2. Synonyms: (3R,4S,5R,6R)-6-(N-benzylamino)-3,4,5-tris(benzyloxy)-1,8-nonadiene
    3. CAS NO:358972-70-0
    4. Molecular Formula:
    5. Molecular Weight: 547.737
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 358972-70-0.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,4S,5R,6R)-6-(N-benzylamino)-3,4,5-tris(benzyloxy)-1,8-nonadiene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3R,4S,5R,6R)-6-(N-benzylamino)-3,4,5-tris(benzyloxy)-1,8-nonadiene(358972-70-0)
    11. EPA Substance Registry System: (3R,4S,5R,6R)-6-(N-benzylamino)-3,4,5-tris(benzyloxy)-1,8-nonadiene(358972-70-0)

  • 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: 358972-70-0(Hazardous Substances Data)

358972-70-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 358972-70-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,8,9,7 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 358972-70:
(8*3)+(7*5)+(6*8)+(5*9)+(4*7)+(3*2)+(2*7)+(1*0)=200
200 % 10 = 0
So 358972-70-0 is a valid CAS Registry Number.

358972-70-0Relevant articles and documents

A short synthetic route to the calystegine alkaloids

Skaanderup, Philip R.,Madsen, Robert

, p. 2115 - 2122 (2003)

An efficient strategy is described for the synthesis of enantiopure calystegine alkaloids. The key step employs a zinc-mediated fragmentation of benzyl-protected methyl 6-iodo-glycosides followed by in situ formation of the benzyl imine and Barbier-type allylation with zinc, magnesium, or indium metal. Stereochemistry in the pivotal allylation is controlled by the choice of the metal. The functionalized 1,8-nonadienes, thus formed, are converted into cycloheptenes by ring-closing olefin metathesis. Regioselective hydroboration and oxidation give the corresponding cycloheptanones, which are deprotected to afford the desired calystegines. Hereby, calystegine B2, B3, and B4 are prepared from D-glucose, D-galactose, and D-mannose, respectively. This route constitutes the shortest synthesis of calystegine B2 and gives rise to the first total syntheses of calystegine B3 and B4.

Short syntheses of enantiopure calystegine B2, B3, and B4

Skaanderup,Madsen

, p. 1106 - 1107 (2007/10/03)

Calystegine B2, B3, and B4 have been prepared in 5 steps from the benzyl protected methyl 6-iodoglycopyranosides of glucose, galactose and mannose, respectively, by using a zinc-mediated domino reaction followed by ring-cl

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