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CAS

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791607-96-0

(S)-1-[(R)-2-oxooxazolidin-4-yl]allyl benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 791607-96-0 Structure

  • Basic information

    1. Product Name: (S)-1-[(R)-2-oxooxazolidin-4-yl]allyl benzoate
    2. Synonyms: (S)-1-[(R)-2-oxooxazolidin-4-yl]allyl benzoate
    3. CAS NO:791607-96-0
    4. Molecular Formula:
    5. Molecular Weight: 247.251
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 791607-96-0.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: (S)-1-[(R)-2-oxooxazolidin-4-yl]allyl benzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-1-[(R)-2-oxooxazolidin-4-yl]allyl benzoate(791607-96-0)
    11. EPA Substance Registry System: (S)-1-[(R)-2-oxooxazolidin-4-yl]allyl benzoate(791607-96-0)

  • 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: 791607-96-0(Hazardous Substances Data)

791607-96-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 791607-96-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,1,6,0 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 791607-96:
(8*7)+(7*9)+(6*1)+(5*6)+(4*0)+(3*7)+(2*9)+(1*6)=200
200 % 10 = 0
So 791607-96-0 is a valid CAS Registry Number.

791607-96-0Relevant articles and documents

Stereocontrolled total synthesis of (+)-1-deoxynojirimycin

Danoun, Gregory,Ceccon, Julien,Greene, Andrew E.,Poisson, Jean-Francois

experimental part, p. 4221 - 4224 (2011/02/24)

A highly efficient non-chiral-pool synthesis of (+)-1-deoxynojirimycin has been realized (24% overall yield, 11 steps, complete stereocontrol). A novel one-pot enol ether metathesis/hydroboration/oxidation sequence is used for the selective formation of the all-trans cyclic triol.

Synthesis and biochemical properties of reversible inhibitors of UDP-N-acetylglucosamine 2-epimerase

Al-Rawi, Samy,Hinderlich, Stephan,Reutter, Werner,Giannis, Athanassios

, p. 4366 - 4370 (2007/10/03)

Sialic acids have important biochemical functions in healthy organisms, for example, in embryogenesis, as well as in the spread of diseases like influenza. A key step in the biosynthesis of the sialic acid N-acetylneuraminic acid is the epimerization of 1

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