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tert-butyl ((3S,4S,5S)-4-(benzyloxy)-5-vinyltetrahydrofuran-3-yl)carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1011247-72-5 Structure
  • Basic information

    1. Product Name: tert-butyl ((3S,4S,5S)-4-(benzyloxy)-5-vinyltetrahydrofuran-3-yl)carbamate
    2. Synonyms: tert-butyl ((3S,4S,5S)-4-(benzyloxy)-5-vinyltetrahydrofuran-3-yl)carbamate
    3. CAS NO:1011247-72-5
    4. Molecular Formula:
    5. Molecular Weight: 319.401
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1011247-72-5.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: tert-butyl ((3S,4S,5S)-4-(benzyloxy)-5-vinyltetrahydrofuran-3-yl)carbamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: tert-butyl ((3S,4S,5S)-4-(benzyloxy)-5-vinyltetrahydrofuran-3-yl)carbamate(1011247-72-5)
    11. EPA Substance Registry System: tert-butyl ((3S,4S,5S)-4-(benzyloxy)-5-vinyltetrahydrofuran-3-yl)carbamate(1011247-72-5)
  • 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: 1011247-72-5(Hazardous Substances Data)

1011247-72-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1011247-72-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,1,2,4 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1011247-72:
(9*1)+(8*0)+(7*1)+(6*1)+(5*2)+(4*4)+(3*7)+(2*7)+(1*2)=85
85 % 10 = 5
So 1011247-72-5 is a valid CAS Registry Number.

1011247-72-5Relevant articles and documents

Asymmetric synthesis of Pachastrissamine (Jaspine B) and its diastereomers via η3-allylpalladium intermediates

Passiniemi, Mikko,Koskinen, Ari M. P.

experimental part, p. 1774 - 1783 (2011/05/04)

A short route for the synthesis of Pachastrissamine (Jaspine B), an anhydrosphingosine derivative, and all three of its diastereomers is presented. The route consists of only 9 steps from the commercially available Garner's aldehyde. The furan framework is formed via an η3-allylpalladium intermediate.

Stereoselective total synthesis of pachastrissamine (jaspine B)

Passiniemi, Mikko,Koskinen, Ari M.P.

, p. 980 - 983 (2008/09/17)

A short total synthesis of the cytotoxic natural product pachastrissamine is described. The synthesis includes eight steps starting from Garner's aldehyde and proceeds in 20% overall yield. Pd(0)-mediated intramolecular cyclisation and Ru-mediated cross-metathesis are the key reactions in this sequence.

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