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CAS

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1018784-07-0

C20H13NO2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1018784-07-0 Structure

  • Basic information

    1. Product Name: C20H13NO2
    2. Synonyms:
    3. CAS NO:1018784-07-0
    4. Molecular Formula:
    5. Molecular Weight: 299.329
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1018784-07-0.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: C20H13NO2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C20H13NO2(1018784-07-0)
    11. EPA Substance Registry System: C20H13NO2(1018784-07-0)

  • 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: 1018784-07-0(Hazardous Substances Data)

1018784-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1018784-07-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,8,7,8 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1018784-07:
(9*1)+(8*0)+(7*1)+(6*8)+(5*7)+(4*8)+(3*4)+(2*0)+(1*7)=150
150 % 10 = 0
So 1018784-07-0 is a valid CAS Registry Number.

1018784-07-0Upstream product

1018784-07-0Downstream Products

1018784-07-0Relevant articles and documents

New 7,8-benzoflavanones as potent aromatase inhibitors: Synthesis and biological evaluation

Yahiaoui, Samir,Fagnere, Catherine,Pouget, Christelle,Buxeraud, Jacques,Chulia, Albert-Jose

, p. 1474 - 1480 (2008)

Some natural compounds such as flavonoids are known to possess a moderate inhibitory activity against aromatase, this enzyme being an interesting target for hormone-dependent breast cancer treatment. It has been demonstrated that the modulation of flavonoid skeleton could increase anti-aromatase effect. Therefore, new 7,8-benzoflavanones were synthesized and tested for their activity toward aromatase inhibition. It was observed that the introduction of a benzo ring at position C-7 and C-8 on flavanone skeleton led to new potent aromatase inhibitors, the resulting 7,8-benzoflavanones being until nine times more potent than aminogluthetimide (the first aromatase inhibitor used clinically).

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