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CAS

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1373355-49-7

C23H15NO4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1373355-49-7 Structure

  • Basic information

    1. Product Name: C23H15NO4
    2. Synonyms: C23H15NO4
    3. CAS NO:1373355-49-7
    4. Molecular Formula:
    5. Molecular Weight: 369.376
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1373355-49-7.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: C23H15NO4(CAS DataBase Reference)
    10. NIST Chemistry Reference: C23H15NO4(1373355-49-7)
    11. EPA Substance Registry System: C23H15NO4(1373355-49-7)

  • 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: 1373355-49-7(Hazardous Substances Data)

1373355-49-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1373355-49-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,3,3,5 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1373355-49:
(9*1)+(8*3)+(7*7)+(6*3)+(5*3)+(4*5)+(3*5)+(2*4)+(1*9)=167
167 % 10 = 7
So 1373355-49-7 is a valid CAS Registry Number.

1373355-49-7Relevant articles and documents

One-pot synthesis of 3-methylflavones and their transformation into (E)-3-styrylflavones via Wittig reactions

Rocha, Djenisa H. A.,Pinto, Diana C. G. A.,Silva, Artur M. S.

, p. 2683 - 2686 (2014/01/06)

An efficient one-pot synthesis of 3-methylflavone derivatives is established. Furthermore, their transformation into phosphorus ylides, which are then used in the diastereoselective synthesis of (E)-styrylflavones through Wittig reactions, is also studied

A new synthesis of 5-arylbenzo[c]xanthones from photoinduced electrocyclisation and oxidation of (E)-3-styrylflavones

Rocha, Djenisa H. A.,Pinto, Diana C. G. A.,Silva, Artur M. S.,Patonay, Tamás,Cavaleiro, José A. S.

experimental part, p. 559 - 564 (2012/04/04)

A new synthetic route to 5-arylbenzo[c]xanthones is -established. This was accomplished by use the Heck reaction of 3-bromoflavones with styrene derivatives, leading to (E)-3-styrylflavones with total diastereoselectivity. This transformation was greatly improved under microwave irradiation. The one-pot, photoinduced electrocyclisation of (E)-3-styrylflavones and further in situ oxidation of the cycloadduct leads to 5-arylbenzo[c]xan-thones. Georg Thieme Verlag Stuttgart · New York.

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