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Octahydro-1H,4H,7H-1,3a,6a,9-tetraazaphenalene is a complex organic compound with the molecular formula C10H16N4. It is a derivative of phenalene, a polycyclic aromatic hydrocarbon, with four nitrogen atoms incorporated into its structure. octahydro-1H,4H,7H-1,3a,6a,9-tetraazaphenalene is characterized by its unique arrangement of carbon and nitrogen atoms, forming a ring structure with a central cavity. The presence of nitrogen atoms in the molecule can lead to various chemical and physical properties, such as increased reactivity and potential applications in the synthesis of other nitrogen-containing compounds. Due to its complex structure, octahydro-1H,4H,7H-1,3a,6a,9-tetraazaphenalene may have potential uses in the fields of organic chemistry, materials science, and pharmaceuticals, although further research is needed to explore its specific properties and applications.

7140-43-4

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7140-43-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7140-43-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,4 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7140-43:
(6*7)+(5*1)+(4*4)+(3*0)+(2*4)+(1*3)=74
74 % 10 = 4
So 7140-43-4 is a valid CAS Registry Number.

7140-43-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Octahydro-1H,4H,7H-1,3a,6a,9-tetraazaphenalene

1.2 Other means of identification

Product number -
Other names trans-Vaccinic acid

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:7140-43-4 SDS

7140-43-4Downstream Products

7140-43-4Relevant academic research and scientific papers

Selectively functionalized constrained polyazamacrocycles: Building blocks for multifunctional chelating agents

Desogere, Pauline,Bernhard, Claire,Goze, Christine,Penouilh, Marie-Jose,Rousselin, Yoann,Denat, Franck

, p. 1538 - 1545 (2013)

A new class of cross-bridged and side-bridged 1,4,7,10- tetraazacyclotridecanes (homocyclens) bearing an aminomethyl pendant arm on the carbon skeleton has been prepared. The regioselectivity of the quaternization of the bis-aminal intermediates is discus

Method of preparing nitrogen macrocycles

-

Page/Page column 12, (2008/06/13)

The invention relates to a method of preparing nitrogen macrocycles having formula (I). The inventive method comprises a step involving the reaction of compounds (II) and (III) in order to form a compound having formula (IV). Said compound is subsequently

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