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1427016-81-6

2,3,4,5-tetra-O-benzyl-D-altrose propane-1,3-diyl dithioacetal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 2,3,4,5-tetra-O-benzyl-D-altrose propane-1,3-diyl dithioacetal

    Cas No: 1427016-81-6

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  • 1427016-81-6 Structure

  • Basic information

    1. Product Name: 2,3,4,5-tetra-O-benzyl-D-altrose propane-1,3-diyl dithioacetal
    2. Synonyms: 2,3,4,5-tetra-O-benzyl-D-altrose propane-1,3-diyl dithioacetal
    3. CAS NO:1427016-81-6
    4. Molecular Formula:
    5. Molecular Weight: 630.869
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1427016-81-6.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: 2,3,4,5-tetra-O-benzyl-D-altrose propane-1,3-diyl dithioacetal(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,3,4,5-tetra-O-benzyl-D-altrose propane-1,3-diyl dithioacetal(1427016-81-6)
    11. EPA Substance Registry System: 2,3,4,5-tetra-O-benzyl-D-altrose propane-1,3-diyl dithioacetal(1427016-81-6)

  • 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: 1427016-81-6(Hazardous Substances Data)

1427016-81-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1427016-81-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,7,0,1 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1427016-81:
(9*1)+(8*4)+(7*2)+(6*7)+(5*0)+(4*1)+(3*6)+(2*8)+(1*1)=136
136 % 10 = 6
So 1427016-81-6 is a valid CAS Registry Number.

1427016-81-6Relevant articles and documents

General synthesis of sugar-derived azepane nitrones: Precursors of azepane iminosugars

Zhao, Wen-Bo,Nakagawa, Shinpei,Kato, Atsushi,Adachi, Isao,Jia, Yue-Mei,Hu, Xiang-Guo,Fleet, George W. J.,Wilson, Francis X.,Horne, Graeme,Yoshihara, Akihide,Izumori, Ken,Yu, Chu-Yi

, p. 3208 - 3221 (2013/06/27)

A general and efficient method has been developed for the synthesis of sugar-derived azepane nitrones starting from aldohexoses, with an intramolecular condensation of aldehyde and hydroxylamine as the key step. Through this strategy, each aldohexose produced a pair of azepane nitrones, which are precursors of various azepane iminosugars.

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