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CAS

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848601-07-0

6,8-Dioxa-3-azabicyclo[3.2.1]octane-7-carboxylic acid, (1R,5R,7R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 848601-07-0 Structure

  • Basic information

    1. Product Name: 6,8-Dioxa-3-azabicyclo[3.2.1]octane-7-carboxylic acid, (1R,5R,7R)-
    2. Synonyms:
    3. CAS NO:848601-07-0
    4. Molecular Formula: C6H9NO4
    5. Molecular Weight:
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 848601-07-0.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: 6,8-Dioxa-3-azabicyclo[3.2.1]octane-7-carboxylic acid, (1R,5R,7R)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6,8-Dioxa-3-azabicyclo[3.2.1]octane-7-carboxylic acid, (1R,5R,7R)-(848601-07-0)
    11. EPA Substance Registry System: 6,8-Dioxa-3-azabicyclo[3.2.1]octane-7-carboxylic acid, (1R,5R,7R)-(848601-07-0)

  • 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: 848601-07-0(Hazardous Substances Data)

848601-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 848601-07-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,6,0 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 848601-07:
(8*8)+(7*4)+(6*8)+(5*6)+(4*0)+(3*1)+(2*0)+(1*7)=180
180 % 10 = 0
So 848601-07-0 is a valid CAS Registry Number.

848601-07-0Downstream Products

848601-07-0Relevant articles and documents

Enantiospecific synthesis of 3-aza-6,8-dioxa-bicyclo[3.2.1]octane carboxylic acids from erythrose

Trabocchi, Andrea,Menchi, Gloria,Rolla, Massimo,Machetti, Fabrizio,Bucelli, Ilaria,Guarna, Antonio

, p. 5251 - 5258 (2003)

New methodology for the synthesis of enantiopure 3-aza-6,8-dioxa-bicyclo[3.2.1]octane-carboxylic acids belonging to 7-endo-BTAa sub-class of γ/δ amino acids is described. The novelty is the use of 2,3-O-isopropylidene-erythrose instead of meso-tartaric ac

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