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  • 1007567-04-5 Structure
  • Basic information

    1. Product Name: C30H31N3O6
    2. Synonyms: C30H31N3O6
    3. CAS NO:1007567-04-5
    4. Molecular Formula:
    5. Molecular Weight: 529.593
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1007567-04-5.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: C30H31N3O6(CAS DataBase Reference)
    10. NIST Chemistry Reference: C30H31N3O6(1007567-04-5)
    11. EPA Substance Registry System: C30H31N3O6(1007567-04-5)
  • 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: 1007567-04-5(Hazardous Substances Data)

1007567-04-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1007567-04-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,7,5,6 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1007567-04:
(9*1)+(8*0)+(7*0)+(6*7)+(5*5)+(4*6)+(3*7)+(2*0)+(1*4)=125
125 % 10 = 5
So 1007567-04-5 is a valid CAS Registry Number.

1007567-04-5Downstream Products

1007567-04-5Relevant articles and documents

Design and synthesis of 4-quinolinone 2-carboxamides as calpain inhibitors

Nam, Dong Hyuk,Lee, Kwang Seob,Kim, Sang Hoon,Kim, Sung Min,Jung, Seo Yun,Chung, Sung Hyun,Kim, Hyoung Ja,Kim, Nam Doo,Jin, Changbae,Lee, Yong Sup

, p. 205 - 209 (2008/09/17)

Calpains are involved in a variety of calcium-regulated cellular processes, such as signal transduction, cell proliferation, differentiation, and apoptosis. Excessive calpain activation contributes to serious cellular damage and has been reported in many pathological conditions. 4-Quinolinone 2-carboxamide derivatives were prepared and evaluated for μ-calpain inhibitory activities. Of the compounds synthesized, 3a and 3k, which possess a primary amide and 4-methoxyphenethyl amide at P1′ region, were found to most potently inhibit μ-calpain with IC50 values of 0.71 ± 0.07 and 0.73 ± 0.23 μM, respectively. On the other hand, the incorporation of pyridine-containing amides decreased inhibitory activity.

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