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1080028-51-8

C14H14O5 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1080028-51-8 Structure

  • Basic information

    1. Product Name: C14H14O5
    2. Synonyms: C14H14O5
    3. CAS NO:1080028-51-8
    4. Molecular Formula:
    5. Molecular Weight: 262.262
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1080028-51-8.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: C14H14O5(CAS DataBase Reference)
    10. NIST Chemistry Reference: C14H14O5(1080028-51-8)
    11. EPA Substance Registry System: C14H14O5(1080028-51-8)

  • 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: 1080028-51-8(Hazardous Substances Data)

1080028-51-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1080028-51-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,0,0,2 and 8 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1080028-51:
(9*1)+(8*0)+(7*8)+(6*0)+(5*0)+(4*2)+(3*8)+(2*5)+(1*1)=108
108 % 10 = 8
So 1080028-51-8 is a valid CAS Registry Number.

1080028-51-8Relevant articles and documents

Synthesis and antiproliferative activity of unnatural enantiomers of 7-epi-goniofufurone and crassalactone C

Popsavin, Velimir,Benedekovic, Goran,Sreco, Bojana,Popsavin, Mirjana,Francuz, Jovana,Kojic, Vesna,Bogdanovic, Gordana

, p. 5178 - 5181 (2008)

A facile synthesis of 7-epi-(-)-goniofufurone as well as the first synthesis of (-)-crassalactone C was achieved starting from d-xylose. A comparison of their in vitro antitumour activities with those observed for the corresponding naturally occurring enantiomers was provided.

Enantiodivergent synthesis of cytotoxic styryl lactones from d-xylose. The first total synthesis of (+)- and (-)-crassalactone C

Popsavin, Velimir,Benedekovi?, Goran,Sre?o, Bojana,Francuz, Jovana,Popsavin, Mirjana,Koji?, Vesna,Bogdanovi?, Gordana,Divjakovi?, Vladimir

experimental part, p. 10596 - 10607 (2010/03/03)

Enantiodivergent total syntheses of both (+)- and (-)-enantiomers of goniofufurone, 7-epi-goniofufurone and crassalactone C have been accomplished starting from d-xylose. The key steps of the synthesis of 7-epi-(+)-goniofufurone were a stereo-selective ad

Design, synthesis and antiproliferative activity of two new heteroannelated (-)-muricatacin mimics

Popsavin, Velimir,Sreco, Bojana,Benedekovic, Goran,Popsavin, Mirjana,Francuz, Jovana,Kojic, Vesna,Bogdanovic, Gordana

scheme or table, p. 5182 - 5185 (2009/05/07)

Two new (-)-muricatacin mimics bearing a furano-furanone ring and an oxygen isostere in the side chain have been designed and synthesized and their in vitro antiproliferative activity was evaluated against several human tumour cell lines. Both analogues showed an increased activity against HL-60 cells with 17- and 185-fold higher potency than (-)-muricatacin. A straightforward synthesis of (-)-muricatacin is also disclosed.

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