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1370556-60-7

C29H40N2O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1370556-60-7 Structure

  • Basic information

    1. Product Name: C29H40N2O2
    2. Synonyms: C29H40N2O2
    3. CAS NO:1370556-60-7
    4. Molecular Formula:
    5. Molecular Weight: 448.649
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1370556-60-7.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: C29H40N2O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C29H40N2O2(1370556-60-7)
    11. EPA Substance Registry System: C29H40N2O2(1370556-60-7)

  • 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: 1370556-60-7(Hazardous Substances Data)

1370556-60-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1370556-60-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,0,5,5 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1370556-60:
(9*1)+(8*3)+(7*7)+(6*0)+(5*5)+(4*5)+(3*6)+(2*6)+(1*0)=157
157 % 10 = 7
So 1370556-60-7 is a valid CAS Registry Number.

1370556-60-7Downstream Products

1370556-60-7Relevant articles and documents

Synthesis and biological evaluation of novel AM80 derivatives as antileukemic agents

Bian, Haiyong,Feng, Jinhong,Xu, Wenfang

, p. 175 - 185 (2013/03/13)

A series of novel AM80 derivatives as antileukemic agents were synthesized and their structures were confirmed by IR, 1H-NMR, and HR-MS spectra. All the target compounds were evaluated for in vitro antiproliferative activities against human leukemic HL-60, NB4, and K562 cell lines. Among these derivatives, compound 4g showed much stronger antiproliferative activities against all the three human leukemic cell lines than the positive control AM80, and compound 4b exhibited more active antiproliferative effects against HL-60 and K562 cells than AM80. Furthermore, the preliminary SAR analysis suggested that AM80 conjugating with HDAC inhibitors with small steric hindrance could give more effective antileukemic agents. These results would be helpful to design more potent antileukemic drugs for the treatment of human leukemia.

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