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110088-79-4

methyl 2-azido-2-deoxy-5-O-p-toluenesulphonyl-α-D-lyxofuranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 110088-79-4 Structure

  • Basic information

    1. Product Name: methyl 2-azido-2-deoxy-5-O-p-toluenesulphonyl-α-D-lyxofuranoside
    2. Synonyms: methyl 2-azido-2-deoxy-5-O-p-toluenesulphonyl-α-D-lyxofuranoside
    3. CAS NO:110088-79-4
    4. Molecular Formula:
    5. Molecular Weight: 343.36
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 110088-79-4.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: methyl 2-azido-2-deoxy-5-O-p-toluenesulphonyl-α-D-lyxofuranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 2-azido-2-deoxy-5-O-p-toluenesulphonyl-α-D-lyxofuranoside(110088-79-4)
    11. EPA Substance Registry System: methyl 2-azido-2-deoxy-5-O-p-toluenesulphonyl-α-D-lyxofuranoside(110088-79-4)

  • 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: 110088-79-4(Hazardous Substances Data)

110088-79-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 110088-79-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,0,8 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 110088-79:
(8*1)+(7*1)+(6*0)+(5*0)+(4*8)+(3*8)+(2*7)+(1*9)=94
94 % 10 = 4
So 110088-79-4 is a valid CAS Registry Number.

110088-79-4Relevant articles and documents

THE SYNTHESIS FROM D-XYLOSE OF THE POTENT AND SPECIFIC ENANTIOMERIC GLUCOSIDASE INHIBITORS, 1,4-DIDEOXY-1,4-IMINO-D-ARABINITOL AND 1,4-DIDEOXY-1,4-AMINO-L-ARABINITOL

Fleet, George W. J.,Smith, Paul W.

, p. 5685 - 5692 (2007/10/02)

Both enantiomers of 1,4-dideoxy-1,4-iminoarabinitol are specific inhibitors of glucosidases.The synthesis of 1,4-dideoxy-1,4-imino-D-arabinitol involves connecting C2 and C5 of xylose together with nitrogen, whereas the synthesis of 1,4-dideoxy-1,4-imino-

POTENT COMPETITIVE INHIBITION OF &α-GALACTOSIDASE AND &α-GLUCOSIDASE ACTIVITY BY 1,4-DIDEOXY-1,4-IMINOPENTITOLS: SYNTHESES OF 1,4-DIDEOXY-1,4-IMINO-D-LYXITOL AND OF BOTH ENANTIOMERS OF 1,4-DIDEOXY-1,4-IMINOARABINITOL

Fleet, G. W. J.,Nicholas, S. J.,Smith, P. W.,Evans, S. V.,Fellows, L. E.,Nash, R. J.

, p. 3127 - 3130 (2007/10/02)

The syntheses of 1,4-dideoxy-1,4-imino-D-lyxitol (3), 1,4-dideoxy-1,4-imino-D-arabinitol (4) and 1,4-dideoxy-1,4-imino-L-arabinitol (5) are reported; (3) is a potent competitive inhibitor of α-galactosidase (green coffee beans) and (4) a competitive inhibitor of α-glucosidase (Brewer's yeast) suggesting that iminopentitols have considerable potential as glycosidase inhibitors. (4) was found to be identical to an alkaloid recently isolated from Angylocalyx boutiqueanus.

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