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714967-70-1

3-O-acetyl-1,2-O-isopropylidene-6-O-trityl-α-L-glucofuranose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 714967-70-1 Structure

  • Basic information

    1. Product Name: 3-O-acetyl-1,2-O-isopropylidene-6-O-trityl-α-L-glucofuranose
    2. Synonyms:
    3. CAS NO:714967-70-1
    4. Molecular Formula:
    5. Molecular Weight: 504.58
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 714967-70-1.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-O-acetyl-1,2-O-isopropylidene-6-O-trityl-α-L-glucofuranose(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-O-acetyl-1,2-O-isopropylidene-6-O-trityl-α-L-glucofuranose(714967-70-1)
    11. EPA Substance Registry System: 3-O-acetyl-1,2-O-isopropylidene-6-O-trityl-α-L-glucofuranose(714967-70-1)

  • 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: 714967-70-1(Hazardous Substances Data)

714967-70-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 714967-70-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,1,4,9,6 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 714967-70:
(8*7)+(7*1)+(6*4)+(5*9)+(4*6)+(3*7)+(2*7)+(1*0)=191
191 % 10 = 1
So 714967-70-1 is a valid CAS Registry Number.

714967-70-1Downstream Products

714967-70-1Relevant articles and documents

Synthesis of calystegine B2, B3, and B4 analogues: Mapping the structure-glycosidase inhibitory activity relationships in the 1-deoxy-6-oxacalystegine series

Garcia-Moreno, M. Isabel,Ortiz Mellet, Carmen,Garcia Fernandez, Jose M.

, p. 1803 - 1819 (2004)

A practical synthesis of ring-modified calystegine analogues with a 6-oxa-nor-tropane structure has been developed. The methodology relies on the ability of the masked carbonyl group of hexose precursors to act as the electrophilic target for the nitrogen

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