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  • 130447-74-4 Structure
  • Basic information

    1. Product Name: C12H20O8
    2. Synonyms:
    3. CAS NO:130447-74-4
    4. Molecular Formula:
    5. Molecular Weight: 292.286
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 130447-74-4.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: C12H20O8(CAS DataBase Reference)
    10. NIST Chemistry Reference: C12H20O8(130447-74-4)
    11. EPA Substance Registry System: C12H20O8(130447-74-4)
  • 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: 130447-74-4(Hazardous Substances Data)

130447-74-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130447-74-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,4,4 and 7 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 130447-74:
(8*1)+(7*3)+(6*0)+(5*4)+(4*4)+(3*7)+(2*7)+(1*4)=104
104 % 10 = 4
So 130447-74-4 is a valid CAS Registry Number.

130447-74-4Downstream Products

130447-74-4Relevant articles and documents

Amylase catalyzed synthesis of glycosyl acrylates and their polymerization

Kloosterman, Wouter M. J.,Jovanovic, Danijela,Brouwer, Sander G. M.,Loos, Katja

, p. 203 - 210 (2014)

The enzymatic synthesis of novel (di)saccharide acrylates from starch and 2-hydroxyethyl acrylate, 2-hydroxyethyl methacrylate and 4-hydroxybutyl acrylate (2-HEA, 2-HEMA and 4-HBA) catalyzed by various commercially available amylase preparations is demonstrated. Both liquefaction and saccharification amylases were tested as biocatalysts. Transglycosidation products were only detected in reaction mixtures containing saccharification amylases. The glycoamylase from Aspergillus niger was found to catalyze the synthesis of 2-(α-glucosyloxy) -ethyl acrylate (Glc-α-EA) from starch. The maltogenic amylase from B. stearothermophilus was found to catalyze the synthesis of 2-(α- maltosyloxy)-ethyl acrylate (Glc-Glc-EA). The transglycosidation product was isolated and purified and its structure was confirmed by 1H-NMR, 13C-NMR and ESI mass spectrometry. The selectivity of the enzyme towards the glycosidation position appeared to be extremely high. Only the anomeric hydroxyl group (C1-OH) of the disaccharide appeared to be glycosidated and the glycosidation products were anomerically pure. Subsequently, the enzymatically synthesized maltosyl acrylate was successfully polymerized by aqueous free radical polymerization to yield a novel acrylic polymer with pendant maltosyl units.

Glycosylation using unprotected alkynyl donors

Mamidyala, Sreeman K.,Finn

experimental part, p. 8417 - 8420 (2010/01/16)

(Chemical Equation Presented) Gold(III) activation of unprotected propargyl glycosyl donors has been shown to be effective for the synthesis of saccharides. Terminal propargyl glycosides of glucose, galactose, and mannose required heating at reflux in ace

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