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1466534-31-5

C11H10N4O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1466534-31-5 Structure

  • Basic information

    1. Product Name: C11H10N4O2
    2. Synonyms:
    3. CAS NO:1466534-31-5
    4. Molecular Formula:
    5. Molecular Weight: 230.226
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1466534-31-5.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: C11H10N4O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C11H10N4O2(1466534-31-5)
    11. EPA Substance Registry System: C11H10N4O2(1466534-31-5)

  • 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: 1466534-31-5(Hazardous Substances Data)

1466534-31-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1466534-31-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,6,6,5,3 and 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1466534-31:
(9*1)+(8*4)+(7*6)+(6*6)+(5*5)+(4*3)+(3*4)+(2*3)+(1*1)=175
175 % 10 = 5
So 1466534-31-5 is a valid CAS Registry Number.

1466534-31-5Downstream Products

1466534-31-5Relevant articles and documents

Three-step synthesis of triazolobenzodiazepinones via sonogashira/huisgen protocol

Molteni, Giorgio

, p. 1765 - 1773 (2013/09/12)

The sequential Sonogashira coupling/intramolecular azide cycloaddition (Huisgen cycloaddition) protocol was performed onto N-(2-iodophenyl)- 2-azidoacetamide as the acyclic precursor giving tricyclic 1,2,3-triazolo- [5,1-d][1,4]benzodiazepin-2-ones. These target products were thus obtained through a three-step synthesis in variable yields depending upon the substituent placed onto the acetylenic counterpart. The influence of catalyst concentration, reaction temperature and reaction medium upon cycloadduct yields were also studied.

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