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105884-24-0

2-Propenoyl azide, 3-(2-nitrophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 105884-24-0 Structure

  • Basic information

    1. Product Name: 2-Propenoyl azide, 3-(2-nitrophenyl)-
    2. Synonyms:
    3. CAS NO:105884-24-0
    4. Molecular Formula: C9H6N4O3
    5. Molecular Weight: 218.172
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 105884-24-0.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: 2-Propenoyl azide, 3-(2-nitrophenyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Propenoyl azide, 3-(2-nitrophenyl)-(105884-24-0)
    11. EPA Substance Registry System: 2-Propenoyl azide, 3-(2-nitrophenyl)-(105884-24-0)

  • 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: 105884-24-0(Hazardous Substances Data)

105884-24-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105884-24-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,8,8 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 105884-24:
(8*1)+(7*0)+(6*5)+(5*8)+(4*8)+(3*4)+(2*2)+(1*4)=130
130 % 10 = 0
So 105884-24-0 is a valid CAS Registry Number.

105884-24-0Upstream product

105884-24-0Relevant articles and documents

Use of the curtius rearrangement of acryloyl azides in the synthesis of 3,5-disubstituted pyridines: Mechanistic studies

Chuang, Ta-Hsien,Chen, Yu-Chi,Pola, Someshwar

supporting information; experimental part, p. 6625 - 6630 (2010/11/18)

A series of disubstituted pyridine derivatives was synthesized from the corresponding acryloyl azides by acetic acid-promoted cycloaddition. This represents a novel and convenient synthetic approach to the symmetric 3,5-disubstituted pyridines. The nature of the substituent on the double bond and the utilized solvent were found to be crucial to the yield of pyridines. The reactivity of the acid-promoted cycloaddition increases with the presence of aryl groups, such as phenyl and pyridinyl. We also explored the comprehensive mechanism by the acid-promoted cycloaddition of 13C-labeled cinnamoyl azide. The symmetric 3,5-disubstituted pyridines were synthesized from acryloyl azides by acetic acid-promoted trimolecular condensation.

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