135825-00-2

Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 18 carbon (C), 28 hydrogen (H), 6 nitrogen (N), and 2 oxygen (O) atoms.
2. Complex organic molecule

Explanation

The compound is classified as a complex organic molecule due to its large size and the presence of multiple functional groups.
3. Cyclic structure of four nitrogen atoms

Explanation

The core structure of the compound consists of a ring formed by four nitrogen atoms, which is characteristic of tetraazacyclododecane.
4. Phenylmethyl group attached to the nitrogen atom

Explanation

A phenylmethyl group (C6H5-CH2-) is attached to one of the nitrogen atoms in the cyclic structure, providing additional complexity to the molecule.
5. Chelating agent

Explanation

The compound is used in coordination chemistry as a chelating agent, which means it can bind to metal ions to form stable coordination complexes.
6. Versatile compound

Explanation

The ability to form stable complexes with a range of metal ions makes 1,4,7,10-Tetraazacyclododecane, 2-[(4-nitrophenyl)methyl]- versatile and important in various chemical applications.
7. Used in pharmaceutical production

Explanation

The compound is utilized in the production of various pharmaceuticals, likely due to its chelating properties and ability to form stable complexes with metal ions.
8. Ligand in organometallic chemistry
9. Nitro group (-NO2) present

Explanation

The compound contains a nitro group attached to the phenyl ring, which is an important functional group that can influence the compound's reactivity and properties.

Upstream product

• 116052-92-7 Toluene-4-sulfonic acid 2-[{2-[{2-[[(S)-3-(4-nitro-phenyl)-2-(toluene-4-sulfonylamino)-propyl]-(toluene-4-sulfonyl)-amino]-ethyl}-(toluene-4-sulfonyl)-amino]-ethyl}-(toluene-4-sulfonyl)-amino]-ethyl ester 
• 116052-91-6 2-(2-{2-[(S)-2-Amino-3-(4-nitro-phenyl)-propylamino]-ethylamino}-ethylamino)-ethanol 
• 17193-40-7 (+)-Methyl 2-amino-3-(4-nitrophenyl)propionate hydrochloride 
• 136169-86-3 3-(4-Nitrobenzyl)-2,6-dioxo-1,4,7,10-tetraazacyclododecane 
• 148436-62-8 2-(4-Nitro-benzyl)-1,4,7,10-tetrakis-(toluene-4-sulfonyl)-1,4,7,10-tetraaza-cyclododecane 
• 136142-46-6 methyl 2-[N-(methoxycarbonylmethyl)amino]-3-(4-nitrophenyl)propionate 

Downstream Products

• 116052-88-1 2-(p-nitrobenzyl)-1,4,7,10-tetraazacyclododecane-N,N',N'',N'''-tetraacetic acid 
• 769138-18-3 C₂₇H₅₃N₅O₁₄P₄ 

Relevant academic research and scientific papers

A New Synthetic Route to 2-(p-Nitrobenzyl)-1,4,7,10-Tetraazacyclododecane

A new, general synthetic method for the title compound has been developed, based on the nitration of 2-benzyl-1,4,7,10-tetraazacyclododecane (64 percent yield), which provides higher yields and easier purification for scale-up than previously reported met

The Peptide Way to Macrocyclic Bifunctional Chelating Agents: Synthesis of 2-(p-Nitrobenzyl)-1,4,7,10-tetraazacyclododecane-N,N',N'',N'''-tetraacetic Acid and Study of Its Yttrium(III) Complex

It was shown that the 12-membered polyazamacrocycle is the favored target for binding trivalent yttrium.We have developed a new synthetic route to these macrocycles via peptide synthesis and intramolecular tosylamide ring closure.