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methyl 5-(5-phenyl-3-isoxazolylmethoxy)pentanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1045792-79-7 Structure
  • Basic information

    1. Product Name: methyl 5-(5-phenyl-3-isoxazolylmethoxy)pentanoate
    2. Synonyms: methyl 5-(5-phenyl-3-isoxazolylmethoxy)pentanoate
    3. CAS NO:1045792-79-7
    4. Molecular Formula:
    5. Molecular Weight: 289.331
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1045792-79-7.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: methyl 5-(5-phenyl-3-isoxazolylmethoxy)pentanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 5-(5-phenyl-3-isoxazolylmethoxy)pentanoate(1045792-79-7)
    11. EPA Substance Registry System: methyl 5-(5-phenyl-3-isoxazolylmethoxy)pentanoate(1045792-79-7)
  • 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: 1045792-79-7(Hazardous Substances Data)

1045792-79-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1045792-79-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,5,7,9 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1045792-79:
(9*1)+(8*0)+(7*4)+(6*5)+(5*7)+(4*9)+(3*2)+(2*7)+(1*9)=167
167 % 10 = 7
So 1045792-79-7 is a valid CAS Registry Number.

1045792-79-7Downstream Products

1045792-79-7Relevant articles and documents

Use of the Nitrile Oxide Cycloaddition (NOC) reaction for molecular probe generation: A new class of enzyme selective histone deacetylase inhibitors (HDACIs) showing picomolar activity at HDAC6

Kozikowski, Alan P.,Tapadar, Subhasish,Luchini, Doris N.,Ki, Hwan Kim,Billadeau, Daniel D.

supporting information; experimental part, p. 4370 - 4373 (2009/05/30)

A series of hydroxamate based HDAC inhibitors containing a phenylisoxazole as the CAP group has been synthesized using nitrile oxide cycloaddition chemistry. An HDAC6 selective inhibitor having a potency of ~2 picomolar was identified. Some of the compounds were examined for their ability to block pancreatic cancer cell growth and found to be about 10-fold more potent than SAHA. This research provides valuable, new molecular probes for use in exploring HDAC biology.

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