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1207869-21-3

C28H28N2O4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1207869-21-3 Structure

  • Basic information

    1. Product Name: C28H28N2O4
    2. Synonyms: C28H28N2O4
    3. CAS NO:1207869-21-3
    4. Molecular Formula:
    5. Molecular Weight: 456.541
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1207869-21-3.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: C28H28N2O4(CAS DataBase Reference)
    10. NIST Chemistry Reference: C28H28N2O4(1207869-21-3)
    11. EPA Substance Registry System: C28H28N2O4(1207869-21-3)

  • 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: 1207869-21-3(Hazardous Substances Data)

1207869-21-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1207869-21-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,7,8,6 and 9 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1207869-21:
(9*1)+(8*2)+(7*0)+(6*7)+(5*8)+(4*6)+(3*9)+(2*2)+(1*1)=163
163 % 10 = 3
So 1207869-21-3 is a valid CAS Registry Number.

1207869-21-3Downstream Products

1207869-21-3Relevant articles and documents

Synthesis and structure based optimization of 2-(4-phenoxybenzoyl)-5- hydroxyindole as a novel CaMKII inhibitor

Komiya, Masafumi,Asano, Shigehiro,Koike, Nobuyuki,Koga, Erina,Igarashi, Junetsu,Nakatani, Shogo,Isobe, Yoshiaki

, p. 6840 - 6847 (2013/01/15)

Based on 2-(4-phenoxybenzoyl)-5-hydroxyindole (2), a novel structural class of CaMKII inhibitors were synthesized and further optimized. The strong acidity of the hydroxyl group and the lipophilic group at the 4 and 6-positions were found to be necessary for strong CaMKII inhibition. Compound 25 was identified as a promising compound with 50-fold more potent inhibitory activity for CaMKII than 2. Compound 25 also showed high selectivity for CaMKII over off-target kinases.

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