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CAS

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1365092-22-3

1,5-anhydro-3,4,6-tri-O-benzyl-2-deoxy-2-(3-pyridinyl)-D-lyxo-hex-1-enitol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1365092-22-3 Structure

  • Basic information

    1. Product Name: 1,5-anhydro-3,4,6-tri-O-benzyl-2-deoxy-2-(3-pyridinyl)-D-lyxo-hex-1-enitol
    2. Synonyms: 1,5-anhydro-3,4,6-tri-O-benzyl-2-deoxy-2-(3-pyridinyl)-D-lyxo-hex-1-enitol
    3. CAS NO:1365092-22-3
    4. Molecular Formula:
    5. Molecular Weight: 493.602
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1365092-22-3.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: 1,5-anhydro-3,4,6-tri-O-benzyl-2-deoxy-2-(3-pyridinyl)-D-lyxo-hex-1-enitol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,5-anhydro-3,4,6-tri-O-benzyl-2-deoxy-2-(3-pyridinyl)-D-lyxo-hex-1-enitol(1365092-22-3)
    11. EPA Substance Registry System: 1,5-anhydro-3,4,6-tri-O-benzyl-2-deoxy-2-(3-pyridinyl)-D-lyxo-hex-1-enitol(1365092-22-3)

  • 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: 1365092-22-3(Hazardous Substances Data)

1365092-22-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1365092-22-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,5,0,9 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1365092-22:
(9*1)+(8*3)+(7*6)+(6*5)+(5*0)+(4*9)+(3*2)+(2*2)+(1*2)=153
153 % 10 = 3
So 1365092-22-3 is a valid CAS Registry Number.

1365092-22-3Downstream Products

1365092-22-3Relevant articles and documents

Phosphine-free suzuki-miyaura cross-coupling in aqueous media enables access to 2-C-aryl-glycosides

Cobo, Isidro,Matheu, M. Isabel,Castillon, Sergio,Boutureira, Omar,Davis, Benjamin G.

, p. 1728 - 1731 (2012/06/18)

A general strategy for the synthesis of 2-aryl-glycals and their elaboration to 2-C-aryl-α-glycosides and 1,5-anhydro-2-C-aryl-2-deoxy alditols are described. The use of reliable, efficient phosphine-free Suzuki-Miyaura cross-coupling of 2-iodoglycals in

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