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51362-37-9

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51362-37-9 Usage

General Description

2-(4-Chlorophenoxy)nicotinic acid is a chemical compound with the molecular formula C12H8ClNO3. It is a derivative of nicotinic acid and contains a chlorophenyl group attached to the nicotinic acid molecule. 2-(4-CHLOROPHENOXY)NICOTINIC ACID has potential applications in pharmaceuticals and agrochemicals due to its ability to act as a ligand for specific receptors in the human body and its pesticidal properties. It is being studied for its potential use in treating various diseases, including cancer and inflammation. Additionally, it has shown promise as a herbicide for controlling unwanted vegetation. The chemical's structure and properties make it a versatile and potentially valuable compound with a range of potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 51362-37-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,3,6 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 51362-37:
(7*5)+(6*1)+(5*3)+(4*6)+(3*2)+(2*3)+(1*7)=99
99 % 10 = 9
So 51362-37-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H8ClNO3/c13-8-3-5-9(6-4-8)17-11-10(12(15)16)2-1-7-14-11/h1-7H,(H,15,16)

51362-37-9 Well-known Company Product Price

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  • Alfa Aesar

  • (A14359)  2-(4-Chlorophenoxy)nicotinic acid, 98%   

  • 51362-37-9

  • 1g

  • 204.0CNY

  • Detail
  • Alfa Aesar

  • (A14359)  2-(4-Chlorophenoxy)nicotinic acid, 98%   

  • 51362-37-9

  • 5g

  • 665.0CNY

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51362-37-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-chlorophenoxy)pyridine-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-(4-Chlorphenoxy)nicotinsaeure

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:51362-37-9 SDS

51362-37-9Relevant articles and documents

Design, Synthesis, and Herbicidal Activity of Novel Diphenyl Ether Derivatives Containing Fast Degrading Tetrahydrophthalimide

Cheng, Yuan,Fu, Ying,Gao, Shuang,Hu, Jia-Jun,Jiang, Mao-Jun,Ren, Tao,Ye, Fei,Zhao, Li-Xia,Zou, Yue-Li

, p. 3729 - 3741 (2020/04/09)

To seek new protoporphyrinogen oxidase (PPO) inhibitors with better biological activity, a series of novel diphenyl ether derivatives containing tetrahydrophthalimide were designed based on the principle of substructure splicing and bioisomerization. PPO inhibition experiments exhibited that 6c is the most potential compound, with the half-maximal inhibitory concentration (IC50) value of 0.00667 mg/L, showing 7 times higher activity than Oxyfluorfen (IC50 = 0.0426 mg/L) against maize PPO and similar herbicidal activities to Oxyfluorfen in weeding experiments in greenhouses and field weeding experiments. In view of the inspected bioactivities, the structure-activity relationship (SAR) of this series of compounds was also discussed. Crop selection experiments demonstrate that compound 6c is safe for soybeans, maize, rice, peanuts, and cotton at a dose of 300 g ai/ha. Accumulation analysis experiments showed that the accumulation of 6c in some crops (soybeans, peanuts, and cotton) was significantly lower than Oxyfluorfen. Current work suggests that compound 6c may be developed as a new herbicide candidate in fields.

Activation and inhibition of kidney CLC-K chloride channels by fenamates

Liantonio, Antonella,Picollo, Alessandra,Babini, Elena,Carbonara, Giuseppe,Fracchiolla, Giuseppe,Loiodice, Fulvio,Tortorella, Vincenzo,Pusch, Michael,Camerino, Diana Conte

, p. 165 - 173 (2007/10/03)

CLC-K Cl- channels are selectively expressed in kidney and ear, where they are pivotal for salt homeostasis, and loss-offunction mutations of CLC-Kb produce Bartter's syndrome type III. The only ligand known for CLC-K channels is a derivative o

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