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2-(3,5-dihydroxyphenyl)-1H-isoindole-1,3(2H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54845-07-7

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54845-07-7 Usage

Chemical class

Isoindole-1,3(2H)-dione, which is a heterocyclic compound.

Structure

Contains a phenyl group and dihydroxy functionality on the isoindole ring.

Functional groups

3,5-dihydroxyphenyl side chain attached to the isoindole-1,3(2H)-dione core.

Potential properties

Antioxidant and medicinal properties due to the presence of the phenyl group and dihydroxy functionality.

Therapeutic applications

Studied for potential use in medicine and pharmaceuticals.

Research interest

Unique structure and properties make it an interesting compound for further research.

Future applications

Possible use in various industries due to its distinct chemical and physical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 54845-07-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,8,4 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 54845-07:
(7*5)+(6*4)+(5*8)+(4*4)+(3*5)+(2*0)+(1*7)=137
137 % 10 = 7
So 54845-07-7 is a valid CAS Registry Number.

54845-07-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3,5-dihydroxyphenyl)isoindole-1,3-dione

1.2 Other means of identification

Product number -
Other names 5-Phthalimido-resorcin

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:54845-07-7 SDS

54845-07-7Relevant academic research and scientific papers

Transfer, amplification, and inversion of helical chirality mediated by concerted interactions of C3-supramolecular dendrimers

Peterca, Mihai,Imam, Mohammad R.,Ahn, Cheol-Hee,Balagurusamy, Venkatachalapathy S. K.,Wilson, Daniela A.,Rosen, Brad M.,Percec, Virgil

, p. 2311 - 2328 (2011/04/23)

The synthesis, structural, and retrostructural analysis of two libraries containing 16 first and second generation C3-symmetric self-assembling dendrimers based on dendrons connected at their apex via trisesters and trisamides of 1,3,5-benzenetricarboxylic acid is reported. A combination of X-ray diffraction and CD/UV analysis methods demonstrated that their C3-symmetry modulates different degrees of packing on the periphery of supramolecular structures that are responsible for the formation of chiral helical supramolecular columns and spheres self-organizable in a diversity of three-dimensional (3D) columnar, tetragonal, and cubic lattices. Two of these periodic arrays, a 3D columnar hexagonal superlattice and a 3D columnar simple orthorhombic chiral lattice with P2221 symmetry, are unprecedented for supramolecular dendrimers. A thermal-reversible inversion of chirality was discovered in helical supramolecular columns. This inversion is induced, on heating, by the change in symmetry from a 3D columnar simple orthorhombic chiral lattice to a 3D columnar hexagonal array and, on cooling, by the change in symmetry from a 2D hexagonal to a 2D centered rectangular lattice, both exhibiting intracolumnar order. A first-order transition from coupled columns with long helical pitch, to weakly or uncorrelated columns with short helical pitch that generates a molecular rotator, was also discovered. The torsion angles of the molecular rotator are proportional to the change in temperature, and this effect is amplified in the case of the C 3-symmetric trisamide supramolecular dendrimers forming H-bonds along their column. The structural changes reported here can be used to design complex functions based on helical supramolecular dendrimers with different degree of packing on their periphery.

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