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1,14-Diazacyclohexacosane-2,15-dione is a complex organic compound with the molecular formula C22H44N2O2. It is a cyclic molecule containing 22 carbon atoms, 2 nitrogen atoms, and 2 oxygen atoms. The compound is characterized by its unique structure, featuring a 26-membered ring with two nitrogen atoms incorporated into the ring, and two carbonyl groups (C=O) at positions 2 and 15. This chemical is not commonly found in nature and is typically synthesized for specific applications in the fields of chemistry and materials science. Due to its large ring structure and the presence of nitrogen and oxygen atoms, 1,14-diazacyclohexacosane-2,15-dione may exhibit unique properties and reactivity, making it a subject of interest for researchers studying the synthesis and potential applications of large cyclic compounds.

4272-08-6

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4272-08-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4272-08-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,7 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4272-08:
(6*4)+(5*2)+(4*7)+(3*2)+(2*0)+(1*8)=76
76 % 10 = 6
So 4272-08-6 is a valid CAS Registry Number.

4272-08-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,14-diazacyclohexacosane-2,15-dione

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4272-08-6 SDS

4272-08-6Downstream Products

4272-08-6Relevant academic research and scientific papers

From Azido Acids to Macrolactams and Macrolactones

Bartra, Marti,Bou, Valenti,Garcia, Jordi,Urpi, Felix,Vilarrasa, Jaume

, p. 270 - 272 (2007/10/02)

A new method is reported for the conversion of azido acids into lactams, via thioester formation and in situ azide reduction and cyclisation under high-dilution conditions; since the quantitative conversion of macrolactams to macrolactones has been shown to be feasible, this results in an indirect, alternative macrolactonisation procedure.

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