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(5-(4-methoxybenzyloxy)-4-oxo-4H-pyran-2-yl)methyl methanesulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 898045-00-6 Structure
  • Basic information

    1. Product Name: (5-(4-methoxybenzyloxy)-4-oxo-4H-pyran-2-yl)methyl methanesulfonate
    2. Synonyms: (5-(4-methoxybenzyloxy)-4-oxo-4H-pyran-2-yl)methyl methanesulfonate
    3. CAS NO:898045-00-6
    4. Molecular Formula:
    5. Molecular Weight: 340.354
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 898045-00-6.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: (5-(4-methoxybenzyloxy)-4-oxo-4H-pyran-2-yl)methyl methanesulfonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (5-(4-methoxybenzyloxy)-4-oxo-4H-pyran-2-yl)methyl methanesulfonate(898045-00-6)
    11. EPA Substance Registry System: (5-(4-methoxybenzyloxy)-4-oxo-4H-pyran-2-yl)methyl methanesulfonate(898045-00-6)
  • 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: 898045-00-6(Hazardous Substances Data)

898045-00-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 898045-00-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,8,0,4 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 898045-00:
(8*8)+(7*9)+(6*8)+(5*0)+(4*4)+(3*5)+(2*0)+(1*0)=206
206 % 10 = 6
So 898045-00-6 is a valid CAS Registry Number.

898045-00-6Relevant articles and documents

Synthesis of tyrosinase inhibitory kojic acid derivative

Lee, Yong Sup,Park, Jang Hyun,Kim, Min Hwan,Seo, Seon Hee,Kim, Hyoung Ja

, p. 111 - 114 (2006)

Kojic acid derivative 2 was synthesized by joining two pyrone rings through an ethylene linkage by Horner-Emmons reaction of phosphonate 6 with aldehyde 7. The intermediates 6 and 7 were derived from kojic acid. The tyrosinase inhibitory activity of 2 was

NOVEL KOJIC ACID CONJUGATED COMPOUNDS AND THEIR BIOLOGICAL APPLICATIONS

-

Paragraph 0067; 0073-0074, (2016/10/10)

The present invention relates to a novel kojic acid conjugated compound conjugated by a click reaction of kojic acid and an antioxidant derivative, an antioxidant dietary supplement comprising the same, and a composition for external application on skin h

Synthesis of kojic acid-derived copper-chelating apoptosis inducing agents

Chen, Yu-Hua,Lu, Pei-Jung,Hulme, Christopher,Shaw, Arthur Y.

, p. 995 - 1003 (2013/04/24)

Three classes of kojic acid derivatives were synthesized and examined for their antiproliferative activity against HeLa cells. Both 8b and 11 co-treated with copper ion exhibited synergistic effect on the HeLa cell growth inhibition with GI50 v

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