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2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-N-phenylbenzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106075-26-7

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106075-26-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106075-26-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,0,7 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 106075-26:
(8*1)+(7*0)+(6*6)+(5*0)+(4*7)+(3*5)+(2*2)+(1*6)=97
97 % 10 = 7
So 106075-26-7 is a valid CAS Registry Number.

106075-26-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phthalimido-benzoic acid anilide

1.2 Other means of identification

Product number -
Other names 2-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-N-phenyl-benzamide

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:106075-26-7 SDS

106075-26-7Downstream Products

106075-26-7Relevant articles and documents

Synthesis of pyrimido[2,1-a]isoindolone and isoindolo[2,1-a]quinazolinoneviaintramolecular aza-Prins type reaction

Biswas, Subhamoy,Porashar, Bikoshita,Arandhara, Pallav Jyoti,Saikia, Anil K.

supporting information, p. 11701 - 11704 (2021/11/12)

A novel aza-Prins type cyclization reaction involvingN-acyliminium ions and amides is reported for the synthesis of tetrahydropyrimido[2,1-a]isoindole-2,6-dione and 6,6a-dihydroisoindolo[2,1-a]quinazoline-5,11-dione derivatives in excellent yields. The strategy features inexpensive reagents, mild reaction conditions, and metal-free synthesis of N-heterocyclic frameworks. Further, post-synthetic modification results in the unprecedented formation of its triazole, tetracyclic diazacyclopenta[def]phenanthrene-1,4(9a1H)-dione and carbonyl derivatives.

Acid Azides: Part X - New Synthesis and Decomposition Reactions of Phthalimidobenzoic Acid Azides

Fahmy, A. F. M.,Aly, N. F.,Mohamed, M. M.,Arief, M. M. H.

, p. 308 - 311 (2007/10/02)

The o-, m-, and p-phthalimidobenzoic acid azides (IIa-c) have been synthesized via the reaction of the corresponding acid chlorides (Ia-c) with aq.NaN3 in acetone.The base-catalyzed decomposition of IIa-c with aromatic amines and/or hydrazines shows that

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