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142009-79-8

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142009-79-8 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) atoms, 15 hydrogen (H) atoms, 1 nitrogen (N) atom, and 1 oxygen (O) atom.

Explanation

A chiral molecule is one that cannot be superimposed onto its mirror image. This compound is chiral due to the presence of stereochemistry (5R,6R)-rel-.

Explanation

Stereochemistry refers to the spatial arrangement of atoms in a molecule. In this case, the compound has a specific arrangement of atoms at the 5th and 6th carbon positions, with the R configuration at both positions.

Explanation

A phenylamino group is a functional group consisting of a phenyl ring attached to an amino group (-NH2). In this compound, the phenylamino group is attached to the 6th carbon of the 5,6-dihydro-phenanthrolin-5-ol core.

Explanation

The compound is of interest in the field of pharmaceutical and medicinal chemistry due to its potential to exhibit biological activities and therapeutic properties, which could be useful in the development of new drugs or treatments.

Explanation

As a chelating agent, this compound can form stable complexes with various metal ions, which is useful in analytical chemistry and material science applications.

Explanation

The compound's ability to act as a chelating agent and its potential biological activities make it useful in various fields, including analytical chemistry, material science, and pharmaceutical research.

Chiral Molecule

Yes

Stereochemistry

(5R,6R)-rel-

Phenylamino Group

Attached to the 6th carbon

Pharmaceutical and Medicinal Chemistry Interest

Potential biological activities and therapeutic properties

Chelating Agent

Forms stable complexes with various metal ions

Applications

Analytical chemistry, material science, and pharmaceutical research

Check Digit Verification of cas no

The CAS Registry Mumber 142009-79-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,0,0 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 142009-79:
(8*1)+(7*4)+(6*2)+(5*0)+(4*0)+(3*9)+(2*7)+(1*9)=98
98 % 10 = 8
So 142009-79-8 is a valid CAS Registry Number.

142009-79-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-5-anilino-6-hydroxy-5,6-dihydro-1,10-phenanthroline

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:142009-79-8 SDS

142009-79-8Relevant 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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