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CAS

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101305-33-3

beta-threo-Pentopyranoside, methyl 2-amino-2,3,4-trideoxy-3-fluoro- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • beta-threo-Pentopyranoside, methyl 2-amino-2,3,4-trideoxy-3-fluoro- (9CI)

    Cas No: 101305-33-3

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  • 101305-33-3 Structure

  • Basic information

    1. Product Name: beta-threo-Pentopyranoside, methyl 2-amino-2,3,4-trideoxy-3-fluoro- (9CI)
    2. Synonyms: beta-threo-Pentopyranoside, methyl 2-amino-2,3,4-trideoxy-3-fluoro- (9CI)
    3. CAS NO:101305-33-3
    4. Molecular Formula: C6H12FNO2
    5. Molecular Weight: 149.16
    6. EINECS: N/A
    7. Product Categories: HALIDE
    8. Mol File: 101305-33-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: beta-threo-Pentopyranoside, methyl 2-amino-2,3,4-trideoxy-3-fluoro- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: beta-threo-Pentopyranoside, methyl 2-amino-2,3,4-trideoxy-3-fluoro- (9CI)(101305-33-3)
    11. EPA Substance Registry System: beta-threo-Pentopyranoside, methyl 2-amino-2,3,4-trideoxy-3-fluoro- (9CI)(101305-33-3)

  • 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: 101305-33-3(Hazardous Substances Data)

101305-33-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101305-33-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,3,0 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 101305-33:
(8*1)+(7*0)+(6*1)+(5*3)+(4*0)+(3*5)+(2*3)+(1*3)=53
53 % 10 = 3
So 101305-33-3 is a valid CAS Registry Number.

101305-33-3Downstream Products

101305-33-3Relevant articles and documents

REACTION DE PARTICIPATION D'AMINES TERTIAIRES ; APPLICATIONS A LA SYNTHESE D'AMINOGLYCOPYRANOSIDES

Picq, D.,Drivas, I.,Carret, G.,Anker, D.,Abou-Assali, M.

, p. 2681 - 2690 (2007/10/02)

Methyl glycopyranosides with diallylamino and mesylate groups in trans relationship undergo an intramolecular reaction in which the amino group assists the replacement of the mesylate group by a nucleophile.Such a reaction may result in a 1,2-shift of the

Synthesis of methyl α- and β-aminofluorodeoxypyranosides

Picq,Anker,Rousset,Laurent

, p. 5619 - 5622 (2007/10/02)

Methyl α,β aminofluorodeoxypyranosides are synthesized in three steps from N,N-diallylaminosugars: O-methanesulfonylation followed with treatment by Et3N,3HF leads to a fluorinated compound; N,N-dideallylation gives the expected product.

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