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6'-O-phenylacetyl-arbutin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1277161-53-1 Structure
  • Basic information

    1. Product Name: 6'-O-phenylacetyl-arbutin
    2. Synonyms: 6'-O-phenylacetyl-arbutin
    3. CAS NO:1277161-53-1
    4. Molecular Formula:
    5. Molecular Weight: 390.39
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1277161-53-1.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: 6'-O-phenylacetyl-arbutin(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6'-O-phenylacetyl-arbutin(1277161-53-1)
    11. EPA Substance Registry System: 6'-O-phenylacetyl-arbutin(1277161-53-1)
  • 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: 1277161-53-1(Hazardous Substances Data)

1277161-53-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1277161-53-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,7,7,1,6 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1277161-53:
(9*1)+(8*2)+(7*7)+(6*7)+(5*1)+(4*6)+(3*1)+(2*5)+(1*3)=161
161 % 10 = 1
So 1277161-53-1 is a valid CAS Registry Number.

1277161-53-1Downstream Products

1277161-53-1Relevant articles and documents

Highly regioselective synthesis of novel aromatic esters of arbutin catalyzed by immobilized lipase from Penicillium expansum

Yang, Rong-Ling,Li, Ning,Ye, Min,Zong, Min-Hua

experimental part, p. 41 - 44 (2010/12/19)

Ester derivatives of phenolic glycosides have attracted more attention in food, cosmetic and pharmaceutical industries, due to their potent biological activities. In the present study, a group of novel aromatic esters of arbutin were successfully synthesized by using immobilized lipase from Penicillium expansum with excellent 6′-regioselectivities (>99%) and moderate to excellent isolated yields (68-93%), except for 6′-O-vanilloyl-arbutin and 6′-O-(p-hydroxycinnamoyl)-arbutin with 28% and 34% yields, respectively. Among all the acyl donors tested, the lipase was most active towards vinyl 3-phenylpropionate, while remarkable decrease in the activity was recorded when the phenyl of acyl donors carried the hydroxyl and/or methoxyl.

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