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125262-43-3

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125262-43-3 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 27 carbon (C) atoms, 30 hydrogen (H) atoms, and 4 nitrogen (N) atoms.

Explanation

This term describes the specific arrangement of atoms in the compound, including the presence of a triazonine ring and three phenylmethyl groups attached to the nitrogen atoms.
3. Heterocyclic compound

Explanation

A heterocyclic compound is a cyclic compound containing atoms of at least two different elements, in this case, carbon, hydrogen, and nitrogen.
4. Chemical Research and Synthesis

Explanation

The compound is primarily used in chemical research and synthesis, which involves studying its properties, reactivity, and potential applications in creating new compounds.
5. Building Block in Organic Chemistry

Explanation

It serves as a starting material or building block for the synthesis of more complex organic compounds, which can be used in various industries, including pharmaceuticals and agrochemicals.
6. Versatile Reactivity

Explanation

The compound is known for its versatile reactivity, meaning it can participate in a wide range of chemical reactions, allowing for the creation of new compounds with diverse properties.
7. Pharmaceutical and Agrochemical Synthesis

Explanation

It is used as a starting material in the synthesis of various pharmaceuticals and agrochemicals, which are chemicals used in the medical and agricultural industries, respectively.
8. Potential Biological Activity

Explanation

The compound has been studied for its potential biological activity, which refers to its ability to interact with living organisms and potentially produce a biological effect.
9. Ongoing Research in Medicinal Chemistry

Explanation

The compound is the subject of ongoing research in medicinal chemistry, a field that focuses on the design, development, and study of drugs and their interactions with biological targets.

Structure

1H-1,4,7-Triazonine, octahydro-1,4,7-tris(phenylmethyl)-

Check Digit Verification of cas no

The CAS Registry Mumber 125262-43-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,2,6 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 125262-43:
(8*1)+(7*2)+(6*5)+(5*2)+(4*6)+(3*2)+(2*4)+(1*3)=103
103 % 10 = 3
So 125262-43-3 is a valid CAS Registry Number.

125262-43-3SDS

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 1,4,7-tribenzyl-1,4,7-triazonane

1.2 Other means of identification

Product number -
Other names N,N',N''-tribenzyl-1,4,7-triazacyclononane

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:125262-43-3 SDS

125262-43-3Relevant articles and documents

From Cyclic Peptoids to Peraza-macrocycles: A General Reductive Approach

Schettini, Rosaria,D'Amato, Assunta,Pierri, Giovanni,Tedesco, Consiglia,Della Sala, Giorgio,Motta, Oriana,Izzo, Irene,De Riccardis, Francesco

, p. 7365 - 7369 (2019/10/02)

Peraza-macrocycles form chelates of high thermodynamic and kinetic stability useful in diagnostic imaging (MRI, SPECT, PET), in coordination chemistry, and as catalysts. In this letter, we report an advantageous method to prepare these compounds via BHsu

An Efficient Synthesis of N,N,N-Substituted 1,4,7-Triazacyclononane

Huang, Yong,Liu, Yajing,Liu, Song,Wu, Renbo,Wu, Zehui

, p. 1546 - 1551 (2018/04/20)

A new and efficient synthetic approach is reported for various N,N,N-substituted 1,4,7-triazacyclononanes (TACN) in moderate to excellent yields, with optimization of the reaction sequences and conditions of the intermediate 1,4,7-tribenzyl-1,4,7-triazonane-2,6-dione reduction with LiAlH4, removal of benzyl with Pd/C, and alkylation reactions. This reaction scheme provides a convenient and flexible method to prepare various N,N,N-substituted TACN derivatives.

SYNTHESIS OF IMIDAZO[1,2-a]PYRAZIN-4-IUM SALTS FOR THE SYNTHESIS OF 1,4,7-TRIAZACYCLONONANE (TACN) AND N- AND/OR C-FUNCTIONALIZED DERIVATIVES THEREOF

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Paragraph 0273; 0274, (2014/05/25)

The present invention embodiments relate to a compound with formula (V′) The invention also relates in certain embodiments to the synthesis method for compound (V′) and its use for the preparation of 1,4,7-triazacyclononane (tacn) and N- and/or C-functionalized derivatives thereof, particularly compounds with formula (I) The invention also relates in certain embodiments to metallic complexes comprising a ligand with formula (I) and a metal and their use for imaging.

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