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132142-67-7

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132142-67-7 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

The chemical structure describes the arrangement of atoms and the type of chemical bonds present in the compound.

Explanation

Phenanthroline is the parent compound from which 1,10-Phenanthrolin-5(6H)-one, 6-[(2-iodophenyl)imino]is derived.

Explanation

The compound's unique structure and properties make it suitable for use in various chemical fields, including the formation of metal complexes.

Explanation

The compound's structure may be utilized in the development of new drugs or pharmaceuticals due to its potential interactions with biological systems.

Explanation

The compound may have potential applications in various other fields of chemical research and development, such as materials science or environmental chemistry.

Explanation

The iodine atom in the phenyl ring contributes to the compound's unique properties and potential applications.

Explanation

The imine functional group is an important structural feature of the compound, which may influence its reactivity and potential applications.

Explanation

A heterocycle is a ring structure containing more than one type of atom, in this case, carbon, nitrogen, and oxygen.

Explanation

The compound is classified as an organic compound due to the presence of carbon and hydrogen atoms in its structure.

Chemical Structure

Phenanthroline core with an imine functional group attached to a phenyl ring substituted with an iodine atom.

Derivative of Phenanthroline

Heterocyclic organic compound.

Potential Applications

Coordination chemistry, organic synthesis, and as a ligand for metal complexes.

Uses in Medicinal and Pharmaceutical Chemistry

Possible applications in drug development and design.

Research and Development

Other areas of chemical research and development.

Iodine Substitution

Presence of an iodine atom in the phenyl ring.

Imine Functional Group

A carbon-nitrogen double bond (C=N) within the molecule.

Heterocycle

Contains atoms of different elements in the ring structure.

Organic Compound

Consists of carbon and hydrogen atoms, with possible additional elements.

Check Digit Verification of cas no

The CAS Registry Mumber 132142-67-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,1,4 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 132142-67:
(8*1)+(7*3)+(6*2)+(5*1)+(4*4)+(3*2)+(2*6)+(1*7)=87
87 % 10 = 7
So 132142-67-7 is a valid CAS Registry Number.

132142-67-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(2-iodophenyl)imino-1,10-phenanthrolin-5-one

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:132142-67-7 SDS

132142-67-7Downstream Products

132142-67-7Relevant articles and documents

The synthesis of ascididemin

Moody, Christopher J.,Rees, Charles W.,Thomas, Robert

, p. 3589 - 3602 (2007/10/02)

A short synthsis of the pentacyclic marine alkaloid ascididemin 1 (four steps, 21% yield) from 1,10-phenanthroline 16 is described. The key step, photocyclisation of the quinoneimine 14 in sulphuric acid, is the first such aza stilbene photocyclisation of a quinoneimine. Intermediate 14 is prepared in a single, but low yielding, step from the quinone 4 in an aza Wadsworth-Emmons reaction, or in much better yield from the epoxide 17 by treatment with 2- iodoaniline and triethylaluminium, followed by oxidation with barium manganate.

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