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C25H23N3O4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1350557-95-7 Structure
  • Basic information

    1. Product Name: C25H23N3O4
    2. Synonyms: C25H23N3O4
    3. CAS NO:1350557-95-7
    4. Molecular Formula:
    5. Molecular Weight: 429.475
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1350557-95-7.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: C25H23N3O4(CAS DataBase Reference)
    10. NIST Chemistry Reference: C25H23N3O4(1350557-95-7)
    11. EPA Substance Registry System: C25H23N3O4(1350557-95-7)
  • 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: 1350557-95-7(Hazardous Substances Data)

1350557-95-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1350557-95-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,0,5,5 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1350557-95:
(9*1)+(8*3)+(7*5)+(6*0)+(5*5)+(4*5)+(3*7)+(2*9)+(1*5)=157
157 % 10 = 7
So 1350557-95-7 is a valid CAS Registry Number.

1350557-95-7Downstream Products

1350557-95-7Relevant articles and documents

An oxidative cross-dehydrogenative-coupling reaction in water using molecular oxygen as the oxidant: Vanadium catalyzed indolation of tetrahydroisoquinolines

Alagiri, Kaliyamoorthy,Kumara, Guralamatta Siddappa Ravi,Prabhu, Kandikere Ramaiah

, p. 11787 - 11789 (2011/11/29)

An aerobic oxidative cross-dehydrogenative coupling reaction between sp3 C-H and sp2 C-H bonds is developed by employing a vanadium catalyst (10 mol%) in an aqueous medium using molecular oxygen as the oxidant. This environmentally benign strategy exhibits larger substrate scope and shows high regioselectivity.

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