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55221-54-0

1,3,4,5-tetra-O-acetylhex-2-ulopyranose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 55221-54-0 Structure

  • Basic information

    1. Product Name: 1,3,4,5-tetra-O-acetylhex-2-ulopyranose
    2. Synonyms:
    3. CAS NO:55221-54-0
    4. Molecular Formula: C14H20O10
    5. Molecular Weight: 348.3026
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 55221-54-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 420.3°C at 760 mmHg
    3. Flash Point: 146.4°C
    4. Appearance: N/A
    5. Density: 1.34g/cm3
    6. Vapor Pressure: 7.97E-09mmHg at 25°C
    7. Refractive Index: 1.493
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1,3,4,5-tetra-O-acetylhex-2-ulopyranose(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1,3,4,5-tetra-O-acetylhex-2-ulopyranose(55221-54-0)
    12. EPA Substance Registry System: 1,3,4,5-tetra-O-acetylhex-2-ulopyranose(55221-54-0)

  • 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: 55221-54-0(Hazardous Substances Data)

55221-54-0 Usage

Chemical structure

A six-carbon sugar molecule (hex-2-ulopyranose) with four acetyl groups (CH3CO-) attached to the hydroxyl (OH) groups on carbons 1, 3, 4, and 5 of the sugar ring.

Derivative

A derivative of hex-2-ulopyranose, a six-carbon sugar molecule.

Functional groups

Contains acetyl groups (CH3CO-) and hydroxyl (OH) groups.

Reactivity

The acetyl groups present in the compound play an important role in its reactivity.

Applications

Commonly used in organic synthesis as a building block for the synthesis of more complex carbohydrate derivatives and as a precursor for the preparation of other organic molecules.

Importance

Valuable starting material for the creation of new chemical compounds due to its reactivity and functional groups.

Check Digit Verification of cas no

The CAS Registry Mumber 55221-54-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,2,2 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 55221-54:
(7*5)+(6*5)+(5*2)+(4*2)+(3*1)+(2*5)+(1*4)=100
100 % 10 = 0
So 55221-54-0 is a valid CAS Registry Number.

55221-54-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (3,4,5-triacetyloxy-2-hydroxyoxan-2-yl)methyl acetate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:55221-54-0 SDS

55221-54-0Relevant articles and documents

Synthesis of α-Acyloxynitrones and Reactivity towards Samarium Diiodide

Racine, Emilie,Burchak, Olga N.,Py, Sandrine

, p. 4003 - 4012 (2016)

Upon treatment of fructose-derived nitrone 1 with samarium diiodide, with the aim of inducing its umpolung and coupling with electrophiles, an unexpected β-elimination of the benzyloxy group at C-1 was observed, yielding nitrone 2. The mechanism and scope

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