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1057653-82-3

4,7-anhydro-6,8-di-O-benzyl-2,3,5-trideoxy-1-O-phthalimido-D-ribo-octitol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1057653-82-3 Structure

  • Basic information

    1. Product Name: 4,7-anhydro-6,8-di-O-benzyl-2,3,5-trideoxy-1-O-phthalimido-D-ribo-octitol
    2. Synonyms: 4,7-anhydro-6,8-di-O-benzyl-2,3,5-trideoxy-1-O-phthalimido-D-ribo-octitol
    3. CAS NO:1057653-82-3
    4. Molecular Formula:
    5. Molecular Weight: 501.579
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1057653-82-3.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: 4,7-anhydro-6,8-di-O-benzyl-2,3,5-trideoxy-1-O-phthalimido-D-ribo-octitol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4,7-anhydro-6,8-di-O-benzyl-2,3,5-trideoxy-1-O-phthalimido-D-ribo-octitol(1057653-82-3)
    11. EPA Substance Registry System: 4,7-anhydro-6,8-di-O-benzyl-2,3,5-trideoxy-1-O-phthalimido-D-ribo-octitol(1057653-82-3)

  • 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: 1057653-82-3(Hazardous Substances Data)

1057653-82-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1057653-82-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,7,6,5 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1057653-82:
(9*1)+(8*0)+(7*5)+(6*7)+(5*6)+(4*5)+(3*3)+(2*8)+(1*2)=163
163 % 10 = 3
So 1057653-82-3 is a valid CAS Registry Number.

1057653-82-3Relevant articles and documents

Stereoselective synthesis of C-ketosides by sequential intramolecular hydrogen atom transfer-intermolecular allylation reaction

Martín, Angeles,Pérez-Martín, Inés,Quintanal, Luis M.,Suárez, Ernesto

, p. 5179 - 5181 (2008)

A tandem 1,5 or 1,6 hydrogen atom transfer (HAT)-radical allylation using carbohydrate models is described. The HAT reaction generated a C-glycos-1-yl radical intermediate, which added to allyltri-n-butyltin with high diastereoselectivity, to give C-ketosides with the quaternary carbon carrying two differently functionalized tethers.

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