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N-(2-Benzothiazolyl)phthalimide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60945-03-1

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60945-03-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60945-03-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,9,4 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 60945-03:
(7*6)+(6*0)+(5*9)+(4*4)+(3*5)+(2*0)+(1*3)=121
121 % 10 = 1
So 60945-03-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H8N2O2S/c18-13-9-5-1-2-6-10(9)14(19)17(13)15-16-11-7-3-4-8-12(11)20-15/h1-8H

60945-03-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1,3-benzothiazol-2-yl)isoindole-1,3-dione

1.2 Other means of identification

Product number -
Other names 2-Phthalimino-benzthiazol

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:60945-03-1 SDS

60945-03-1Downstream Products

60945-03-1Relevant academic research and scientific papers

An efficient green synthesis of new benzothiazoles containing sulfonamide or cyclic imide moieties

Bougheloum, Chafika,Alioua, Sabrina,Belghiche, Robila,Benali, Nesma,Messalhi, Abdelrani

supporting information, p. 120 - 131 (2019/12/24)

An efficient and convenient protocol for the one-pot synthesis of new benzothiazoles bearing sulfonamide or cyclic imide moieties using Cesium salt of Wells-Dawson heteropolyacid (Cs5HP2W18O62) as solid catalyst and water as solvent under ultrasound irradiation was reported. The reaction speed was remarkably catalyzed with the aid of ultrasound irradiation. Moreover, this approach prepares multiple other benefits such as operational ease, higher yields, and energy performance.

Thalidomide analogues: Tumor necrosis factor-alpha inhibitors and their evaluation as anti-inflammatory agents

Casal, Juan José,Bollini, Mariela,Lombardo, María Elisa,Bruno, Ana María

, p. 114 - 119 (2016/01/09)

A series of related thalidomide derivatives (2-9) were synthesized by microwave irradiation and evaluated for anti-inflammatory activity. Such activity was assessed in vivo and ex vivo. Compounds 2, 8 and 9 showed the highest levels of inhibition of TNF-α production. On rat paw edema and hyperalgesia assays, compound 9, (1,4-phthalazinedione) demonstrated the highest in vivo anti-inflammatory activity. Thus, compound 9 can be considered as a promising compound to be subjected to further modification to obtain new agents for the treatment of inflammatory diseases.

Synthesis and anti-angiogenic activity of benzothiazole, benzimidazole containing phthalimide derivatives

Nagarajan, Shunmugam,Majumder, Syamantak,Sharma, Upendra,Rajendran, Saranya,Kumar, Neeraj,Chatterjee, Suvro,Singh, Bikram

supporting information, p. 287 - 290 (2013/02/23)

Benzothiazole and benzimidazole containing phthalimide derivatives (NK037, NK041, NK042, NK0139A and NK0148) have been synthesized and their anti-angiogenic activity was evaluated using ex vivo egg yolk angiogenesis model. A comparative study with pure thalidomide (NKTA) has also been performed to describe the efficacy of these derivatives in blocking angiogenesis. NK037, NK041 and NK042 were equally potent in blocking egg yolk angiogenesis and the anti-angiogenesis effect was higher than NKTA suggesting the efficacy of these three derivatives in blocking angiogenesis when compare to control. Other two derivatives NK0139A and NK0148 showed effect less than NKTA and stronger than control in ex vivo angiogenesis.

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