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64044-28-6

1,2,3,4,5-penta-O-acetyl-6-O-methyl-D-galactitol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 64044-28-6 Structure

  • Basic information

    1. Product Name: 1,2,3,4,5-penta-O-acetyl-6-O-methyl-D-galactitol
    2. Synonyms:
    3. CAS NO:64044-28-6
    4. Molecular Formula:
    5. Molecular Weight: 406.387
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 64044-28-6.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: 1,2,3,4,5-penta-O-acetyl-6-O-methyl-D-galactitol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,2,3,4,5-penta-O-acetyl-6-O-methyl-D-galactitol(64044-28-6)
    11. EPA Substance Registry System: 1,2,3,4,5-penta-O-acetyl-6-O-methyl-D-galactitol(64044-28-6)

  • 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: 64044-28-6(Hazardous Substances Data)

64044-28-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64044-28-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,0,4 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 64044-28:
(7*6)+(6*4)+(5*0)+(4*4)+(3*4)+(2*2)+(1*8)=106
106 % 10 = 6
So 64044-28-6 is a valid CAS Registry Number.

64044-28-6Downstream Products

64044-28-6Relevant articles and documents

A facile method for the synthesis of partially O-methylated alditol acetate standards for GC-MS analysis of galactofuranose-containing structures

He, Jian-Yu,Guo, Yu-Na,Zhang, Ling-Ling,Huang, Lin-Hong

, p. 18 - 20 (2013/10/21)

Mixtures of partially O-methylated alditol acetate standards of galactofuranose were synthesized rapidly. Methyl galactofuranosides were obtained with a yield of 79.9% within 4 h under optimized reaction conditions. Methylation of methyl glycosides was carried out in the presence of BaO/Ba(OH)2·8H2O, giving rise to mixtures of partially methylated glycosides. The batch containing the most diverse structures of methyl ethers was converted into partially O-methylated alditol acetates (PMAAs) and then subjected to GC-MS. These PMAAs could be used as GC-MS standards for simultaneous identification of galactofuranose units with diverse linkages in complex carbohydrates.

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