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CAS

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156276-15-2

1-(2-Bromobenzyl)-2,14-dioxo-1-azacyclotetradecan-3-carbonsaeure-allylester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 156276-15-2 Structure

  • Basic information

    1. Product Name: 1-(2-Bromobenzyl)-2,14-dioxo-1-azacyclotetradecan-3-carbonsaeure-allylester
    2. Synonyms: 1-(2-Bromobenzyl)-2,14-dioxo-1-azacyclotetradecan-3-carbonsaeure-allylester
    3. CAS NO:156276-15-2
    4. Molecular Formula:
    5. Molecular Weight: 478.426
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 156276-15-2.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: 1-(2-Bromobenzyl)-2,14-dioxo-1-azacyclotetradecan-3-carbonsaeure-allylester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(2-Bromobenzyl)-2,14-dioxo-1-azacyclotetradecan-3-carbonsaeure-allylester(156276-15-2)
    11. EPA Substance Registry System: 1-(2-Bromobenzyl)-2,14-dioxo-1-azacyclotetradecan-3-carbonsaeure-allylester(156276-15-2)

  • 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: 156276-15-2(Hazardous Substances Data)

156276-15-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156276-15-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,2,7 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 156276-15:
(8*1)+(7*5)+(6*6)+(5*2)+(4*7)+(3*6)+(2*1)+(1*5)=142
142 % 10 = 2
So 156276-15-2 is a valid CAS Registry Number.

156276-15-2Relevant articles and documents

77. Macrocyclic Imides: Versatile Synthons in Ring-Enlargement Reactions

Koch, Thomas,Hesse, Manfred

, p. 819 - 828 (1994)

Macrocyclic imides differ from phthal- or succinimids in their increased electrophilicity.This property makes them versatile synthons for reactions with several nucleophiles.If a nucleophile is attached to the N-substituent of the imide, an intramolecular

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