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3,5-di-O-benzyl-6-deoxy-6-nitro-β-L-idono-1,4-lactone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 848345-33-5 Structure
  • Basic information

    1. Product Name: 3,5-di-O-benzyl-6-deoxy-6-nitro-β-L-idono-1,4-lactone
    2. Synonyms:
    3. CAS NO:848345-33-5
    4. Molecular Formula:
    5. Molecular Weight: 387.389
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 848345-33-5.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: 3,5-di-O-benzyl-6-deoxy-6-nitro-β-L-idono-1,4-lactone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,5-di-O-benzyl-6-deoxy-6-nitro-β-L-idono-1,4-lactone(848345-33-5)
    11. EPA Substance Registry System: 3,5-di-O-benzyl-6-deoxy-6-nitro-β-L-idono-1,4-lactone(848345-33-5)
  • 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: 848345-33-5(Hazardous Substances Data)

848345-33-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 848345-33-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,3,4 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 848345-33:
(8*8)+(7*4)+(6*8)+(5*3)+(4*4)+(3*5)+(2*3)+(1*3)=195
195 % 10 = 5
So 848345-33-5 is a valid CAS Registry Number.

848345-33-5Relevant articles and documents

Stereocontrolled transformation of nitrohexofuranoses into cyclopentylamines via 2-oxabicyclo[2.2.1]heptanes. Part 2: Synthesis of (1S,2R,3S,4S,5R)-3,4,5-trihydroxy-2-aminocyclopentanecarboxylic acid

Soengas, Raquel G.,Begona Pampiin,Estevez, Juan C.,Estevez, Ramon J.

, p. 205 - 211 (2007/10/03)

A recent new strategy for the transformation of nitrohexofuranoses into cyclopentylamines, based on intramolecular cyclization followed by controlled opening of the resulting 2-oxabicyclo[2.2.1]heptane derivatives, allowed the first total synthesis of (1S

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