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98976-24-0

1-(3,4,6-tri-O-benzyl-2-deoxy-α-D-arabino-hexapyranosyl)-1-hexanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 98976-24-0 Structure

  • Basic information

    1. Product Name: 1-(3,4,6-tri-O-benzyl-2-deoxy-α-D-arabino-hexapyranosyl)-1-hexanol
    2. Synonyms:
    3. CAS NO:98976-24-0
    4. Molecular Formula:
    5. Molecular Weight: 518.693
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 98976-24-0.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: 1-(3,4,6-tri-O-benzyl-2-deoxy-α-D-arabino-hexapyranosyl)-1-hexanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(3,4,6-tri-O-benzyl-2-deoxy-α-D-arabino-hexapyranosyl)-1-hexanol(98976-24-0)
    11. EPA Substance Registry System: 1-(3,4,6-tri-O-benzyl-2-deoxy-α-D-arabino-hexapyranosyl)-1-hexanol(98976-24-0)

  • 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: 98976-24-0(Hazardous Substances Data)

98976-24-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98976-24-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,9,7 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 98976-24:
(7*9)+(6*8)+(5*9)+(4*7)+(3*6)+(2*2)+(1*4)=210
210 % 10 = 0
So 98976-24-0 is a valid CAS Registry Number.

98976-24-0Relevant articles and documents

STEREOCONTROLLED PREPARATION OF C-2-DEOXY-α- AND -β-D-GLUCOPYRANOSYL COMPOUNDS FROM TRIBUTYL-(2-DEOXY-α- AND -β-D-GLUCOPYRANOSYL)STANNANES

Lesimple, Patrick,Beau, Jean-Marie,Sinay, Pierre

, p. 289 - 300 (1987)

Tributylstannyllithium treatment of 3,4,6-tri-O-benzyl-2-deoxy-α-D-arabino-hexopyranosyl chloride (2) provided selectively tributyl (3,4,6-tri-O-benzyl-2-deoxy-β-D-arabino-hexopyranosyl)stannane (3) in 85percent yield.Isomeric tributyl (3,4,6-tri-O-benzyl-2-deoxy-α-D-arabino-hexopyranosyl)stannane (6) could be prepared in 70percent yield by reductive lithiation of 2 and reaction with tributyltin chloride.Tin-lithium exchange reaction, performed on 3 and 6 with butyllithium in oxolane at -78 deg C, generated the corresponding, configurationally stable 2-deoxy-β- and -α-D-hexopyranosyllithium compounds which reacted with electrophilic compounds with retention of configuration.Addition of these glycosyllithium reagnts to prochiral carbonyl compounds gave variable degrees of facial selectivity.A significant diastereofacial discrimination (10:1) was observed by condensation of 3,4,6-tri-O-benzyl-2-deoxy-α-D-arabino-hexopyranosyllithium reagent with hexanal and isobutyraldehyde.The structure of all C-glycopyranosyl compounds obtained was established by 1H-n.m.r. spectroscopy.

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