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CAS

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116270-20-3

E-ethyl 3-azidoacrylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 116270-20-3 Structure

  • Basic information

    1. Product Name: E-ethyl 3-azidoacrylate
    2. Synonyms: E-ethyl 3-azidoacrylate
    3. CAS NO:116270-20-3
    4. Molecular Formula:
    5. Molecular Weight: 141.129
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 116270-20-3.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: E-ethyl 3-azidoacrylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: E-ethyl 3-azidoacrylate(116270-20-3)
    11. EPA Substance Registry System: E-ethyl 3-azidoacrylate(116270-20-3)

  • 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: 116270-20-3(Hazardous Substances Data)

116270-20-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116270-20-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,2,7 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 116270-20:
(8*1)+(7*1)+(6*6)+(5*2)+(4*7)+(3*0)+(2*2)+(1*0)=93
93 % 10 = 3
So 116270-20-3 is a valid CAS Registry Number.

116270-20-3Upstream product

116270-20-3Relevant articles and documents

Organic Azides. 5. A Simple Synthesis of Alkyl 3-Azido-2-alkenoates

Priebe, Hanno

, p. 640 - 645 (2007/10/02)

The title compounds are derived from alkyl 2-alkynoates and aqueous sodium azide solution under ultrasonic irradiation.At low reaction temperatures the Z-configuration is favoured.Ultrasonic irradiation is decisive for good conversion and in most cases no additional stirring is necessary.Stirring without ultrasonic irradiation gives low conversion.The reaction conditions show high selectivity between nucleophilic addition and nucleophilic substitution.

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