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methyl 3-(1,3-dioxoisoindolin-2-yl)benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

300667-12-3

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300667-12-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 300667-12-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,0,6,6 and 7 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 300667-12:
(8*3)+(7*0)+(6*0)+(5*6)+(4*6)+(3*7)+(2*1)+(1*2)=103
103 % 10 = 3
So 300667-12-3 is a valid CAS Registry Number.

300667-12-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(3-methoxycarbonylphenyl)phthalimide

1.2 Other means of identification

Product number -
Other names methyl 3-(N-phthalimidyl)benzoate

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:300667-12-3 SDS

300667-12-3Relevant academic research and scientific papers

Synthesis of phthalimides, isoindolin-1-ones and isoindolines bearing aminobenzoic acids as a new fluorescent compounds

Solis-Santos, Melchor,Ordó?ez, Mario,Ochoa-Terán, Adrián,Morales-Cueto, Rodrigo,Labastida-Galván, Victoria

, (2021/03/30)

Both experimental and theoretical methods were used in order to study the fluorescent properties of nine new compounds based on phthalimides, isoindolin-1-ones and isoindolines bearing aminobenzoic acids (2-aminobenzoic acid, 3-aminobenzoic acid and 4-aminobenzoic acid), which were obtained under mild reaction conditions. The photophysical properties of all the compounds were studied by electronic absorption and fluorescence spectroscopy in methanol solutions. All compounds exhibited fluorescence emission and high quantum yields. Additionally, it was found that the intramolecular charge in these donor-acceptor systems is significantly depending on electron-withdrawing substituents at the carboxylic acid position.

Visible-Light-Induced Metal-/Photocatalyst-Free C-H Bond Imidation of Arenes

Kuribara, Takahito,Nakajima, Masaya,Nemoto, Tetsuhiro

supporting information, p. 2235 - 2239 (2020/03/13)

In this study, a visible-light-induced intermolecular C-H bond imidation of arenes was achieved at ambient condition. By using simple phthalimide with (diacetoxyiodo)benzene and molecular iodine, direct metal-/photocatalyst-free C-N bond formation was achieved. The imidation protocol was designed by using time-dependent density functional theory calculations and experimentally demonstrated for 28 substrates with as high as 96% yield. Mechanistic studies indicated that radical-mediated aromatic substitution occurred via photolysis of N-iodophthalimide under visible-light irradiation.

Nitrogen-centered radical-mediated C-H imidation of arenes and heteroarenes via visible light induced photocatalysis

Kim, Hyejin,Kim, Taehoon,Lee, Dong Gil,Roh, Sang Weon,Lee, Chulbom

supporting information, p. 9273 - 9276 (2014/08/05)

The C-H imidation of arenes and heteroarenes has been achieved via visible light induced photocatalysis. In the presence of an iridium(iii) photoredox catalyst, the reaction of aromatic substrates with N-chlorophthalimide furnishes the N-aryl products at room temperature through a nitrogen-centered radical mediated aromatic substitution.

Synthesis and SAR of novel, non-MPEP chemotype mGluR5 NAMs identified by functional HTS

Zhou, Ya,Rodriguez, Alice L.,Williams, Richard,Weaver, C. David,Conn, P. Jeffrey,Lindsley, Craig W.

scheme or table, p. 6502 - 6506 (2010/05/17)

This Letter describes the discovery and SAR of three novel series of mGluR5 non-competitive antagonists/negative allosteric modulators (NAMs) not based on manipulation of an MPEP/MTEP chemotype identified by a functional HTS approach. This work demonstrates fundamentally new mGluR5 NAM chemotypes with submicromolar potencies, and further examples of a mode of pharmacology 'switch' to provide PAMs with a non-MPEP scaffold.

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