Cas 156276-15-2,1-(2-Bromobenzyl)-2,14-dioxo-1-azacyclotetradecan-3-carbonsaeure-allylester

156276-15-2

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Basic information

Product Name: 1-(2-Bromobenzyl)-2,14-dioxo-1-azacyclotetradecan-3-carbonsaeure-allylester
Synonyms: 1-(2-Bromobenzyl)-2,14-dioxo-1-azacyclotetradecan-3-carbonsaeure-allylester
CAS NO:156276-15-2
Molecular Formula:
Molecular Weight: 478.426
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1-(2-Bromobenzyl)-2,14-dioxo-1-azacyclotetradecan-3-carbonsaeure-allylester(CAS DataBase Reference)
NIST Chemistry Reference: 1-(2-Bromobenzyl)-2,14-dioxo-1-azacyclotetradecan-3-carbonsaeure-allylester(156276-15-2)
EPA Substance Registry System: 1-(2-Bromobenzyl)-2,14-dioxo-1-azacyclotetradecan-3-carbonsaeure-allylester(156276-15-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 156276-15-2(Hazardous Substances Data)

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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.

156276-15-2Upstream product

97416-37-0 2-Oxocyclododecan-1-carbonsaeure-allylester

156276-15-2Downstream Products

156276-17-4 1-(2-Bromobenzyl)-1-azacyclotetradecan-2,14-dion

156276-15-2Relevant academic research and scientific papers

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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