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33742-69-7

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33742-69-7 Usage

General Description

6-chloro-N-ethyl-3-nitropyridin-2-amine is a chemical compound with the molecular formula C8H9ClN3O2. It is a derivative of pyridine and contains a nitro group, a chlorine atom, and an ethyl group. 6-chloro-N-ethyl-3-nitropyridin-2-amine is used in the synthesis of pharmaceuticals and agrochemicals, and it may have potential applications in the field of medicinal chemistry. It is important to handle this compound with care, as it may be hazardous if not used properly.

Check Digit Verification of cas no

The CAS Registry Mumber 33742-69-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,7,4 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 33742-69:
(7*3)+(6*3)+(5*7)+(4*4)+(3*2)+(2*6)+(1*9)=117
117 % 10 = 7
So 33742-69-7 is a valid CAS Registry Number.

33742-69-7SDS

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 6-chloro-N-ethyl-3-nitropyridin-2-amine

1.2 Other means of identification

Product number -
Other names -

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:33742-69-7 SDS

33742-69-7Downstream Products

33742-69-7Relevant articles and documents

Synthesis of 2-substituted 3-ethyl-3H-imidazo[4,5-b]pyridines catalyzed by Al3+-exchanged K10 clay as solid acids

Suresh, Dhanusu,Dhakshinamoorthy, Amarajothi,Kanagaraj, Kuppusamy,Pitchumani, Kasi

, p. 6479 - 6484 (2013)

A series of imidazopyridine derivatives have been synthesized efficiently via intramolecular cyclization in excellent yields using Al3+- exchanged on K10 montmorillonite clay (Al3+-K10 clay) as a reusable heterogeneous catalyst. To the best of our knowledge, this is the first report to utilize Al3+-K10 as a catalyst for imidazopyridine synthesis. Many functional groups are tolerated during the synthesis of targeted compounds. The catalyst is reused at least five times with a slight decrease in the yield. This catalyst is environmentally benign, cost-effective, and also provides other advantages such as nontoxicity, operational/experimental simplicity, and mild reaction conditions.

METALLOENZYME INHIBITOR COMPOUNDS

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Paragraph 0549; 0550; 0551; 0552, (2018/07/29)

Provided are compounds having metalloenzyme modulating activity, and methods of treating diseases, disorders or symptoms thereof mediated by such metalloenzymes.

Design, Synthesis, and Fungicidal Activity of Novel Imidazo[4,5-b]pyridine Derivatives

Liu, Minhua,Quan, Chunsheng,Dang, Mingming,Ren, Yeguo,Ren, Jianwei,Xiang, Jun,Liu, Xingping,He, Lian,Liu, Weidong,Liu, Aiping

, p. 2061 - 2068 (2018/07/31)

A series of novel imidazo[4,5-b]pyridine derivatives were designed and synthesized. The structures of all the newly synthesized compounds were identified by spectroscopic data NMR, MS, and elemental analysis. Bioassay showed that the compounds exhibited potent fungicidal activities against Erysiphe graminis, Puccinia polysora, and so forth. Particularly, 2-chloro-5-((5-methoxy-2-(2-(trifluoromethyl)phenyl)-3H-imidazo[4,5-b]pyridin-3-yl)methyl)thiazole (9b) displayed fungicidal potency against P.?polysora. Its EC50 value: 4.00?mg/L is comparable with that of tebuconazole. The structure–activity relationship for the target compounds is discussed.

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