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261761-55-1

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261761-55-1 Usage

General Description

2,3-Dichloro-N'-hydroxybenzenecarboximidamide, also known as diuron, is a chemical compound commonly used as a herbicide to control the growth of unwanted plants. It belongs to the phenylurea class of chemicals and is widely used in agriculture as well as in non-agricultural settings such as industrial sites and residential areas. Diuron works by inhibiting photosynthesis in plants, leading to their eventual death. While effective at controlling weeds, diuron has been found to have detrimental effects on aquatic organisms and is considered a potential environmental hazard. Due to its persistence in the environment and potential for runoff into water sources, the use of diuron is heavily regulated in many countries.

Check Digit Verification of cas no

The CAS Registry Mumber 261761-55-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,1,7,6 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 261761-55:
(8*2)+(7*6)+(6*1)+(5*7)+(4*6)+(3*1)+(2*5)+(1*5)=141
141 % 10 = 1
So 261761-55-1 is a valid CAS Registry Number.

261761-55-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-DICHLORO-N'-HYDROXYBENZENECARBOXIMIDAMIDE

1.2 Other means of identification

Product number -
Other names 2,3-dichloro-N'-hydroxybenzamidine

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:261761-55-1 SDS

261761-55-1Relevant articles and documents

Synthesis and Biological Evaluation of Sigma-1 (σ1) Receptor Ligands Based on Phenyl-1,2,4-oxadiazole Derivatives

Cao, Xudong,Yao, Zhongyuan,Dou, Fei,Zhang, Yifang,Qiu, Yinli,Zhao, Song,Xu, Xiangqing,Liu, Xin,Liu, Bi-Feng,Chen, Yin,Zhang, Guisen

, (2019/02/26)

In this study, a series of phenyl-1,2,4-oxadiazole derivatives were synthesized and evaluated for anti-allodynic activity. Structure–activity relationship studies identified 1-{4-[3-(2,4-dichlorophenyl)-1,2,4-oxadiazol-5-yl]butyl}piperidine (39) with excellent affinity for the σ1 receptor and selectivity for the σ2 receptor, with poor activity to other central nervous system neurotransmitter receptors and transporters associated with pain. Compound 39 exhibited dose-dependent efficacy in suppressing the formalin-induced flinching and attenuating mechanical allodynia in chronic constriction injury-induced neuropathic rats. These results suggest that compound 39 exerts potent antihyperalgesic activity and could be considered as a promising candidate for treating neuropathic pain.

HETEROARYL SUBSTITUTED DIAZABICYCLONONENE DERIVATIVES

-

Page/Page column 15, (2010/11/08)

The invention relates to heteroaryl substituted diazabicyclononene derivatives, related compounds and use thereof as active ingredients in the preparation of pharmaceutical compositions. The invention also concerns related aspects including processes for

Structure-activity relationships of acyloxyamidine cytomegalovirus DNA polymerase inhibitors

Tucker, John A.,Clayton, Terrance L.,Chidester, Connie G.,Schulz, Martin W.,Harrington, Leigh E.,Conrad, Steven J.,Yagi, Yoshihiko,Oien, Nancee L.,Yurek, David,Kuo, Ming-Shang

, p. 601 - 615 (2007/10/03)

This paper describes the structure-activity relationships of a new class of cytomegalovirus DNA polymerase inhibitors having two aryl groups joined by an acyloxyamidine linker. Examination of a series of analogues in which the terminal groups are varied r

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