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3,4,5,6-Tetrahydro-N-(4-chlorophenyl)phthalimide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39985-63-2

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39985-63-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39985-63-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,9,8 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 39985-63:
(7*3)+(6*9)+(5*9)+(4*8)+(3*5)+(2*6)+(1*3)=182
182 % 10 = 2
So 39985-63-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H12ClNO2/c15-9-5-7-10(8-6-9)16-13(17)11-3-1-2-4-12(11)14(16)18/h5-8H,1-4H2

39985-63-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-chlorophenyl)-3,4,5,6-tetrahydrophthalimide

1.2 Other means of identification

Product number -
Other names chlorophthalim

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:39985-63-2 SDS

39985-63-2Downstream Products

39985-63-2Relevant academic research and scientific papers

Hydrolysis and Phytotoxic Activity of Cyclic Imides

Sato, Yukiharu,Kojima, Takashi,Goto, Toshiyuki,Oomikawa, Reiko,Watanabe, Hiroyuki,Wakabayashi, Ko

, p. 2677 - 2682 (2007/10/02)

In order to explain the close phytotoxic activities of N-aryl-3,4,5,6-tetrahydrophthalimides and their hydrolyzed products, N-aryl-3,4,5,6-tetrahydrophthalamic acids, five sets of both types of compounds possessing the same aryl residues were prepared.Their phytotoxic activity against sawa millett (E. utilis) and green microalga (S. acutus), and the relationship of interconversion between the imides and amide acids during the bioassay were investigated.In almost all cases, the imides showed stronger activity than the corresponding amide acids.The hydrolysis of the imides and the cyclization of amide acids were observed in respect of the aryl residues.The phytotoxicity caused by the imides and amide acids tested was influenced by this interconversion.

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