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1-(3-CHLOROPHENYL)-3-(3-(PHENYLMETHOXY)(2-PYRIDYL))UREA is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

877459-37-5

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877459-37-5 Usage

Chemical class

Urea derivative

Explanation

The compound belongs to the urea class of compounds, which are characterized by the presence of a urea functional group (-NH-CO-NH-).

Explanation

The urea molecule has two distinct substituents attached to it, which contribute to its unique properties and potential applications.

Explanation

Due to its unique structure, 1-(3-CHLOROPHENYL)-3-(3-(PHENYLMETHOXY)(2-PYRIDYL))UREA may have potential uses in the fields of medicine (e.g., as a pharmaceutical agent) and agriculture (e.g., as a pesticide or herbicide).

Explanation

To determine the compound's potential uses and effects, further studies on its synthesis and properties are required.

Explanation

Urea derivatives, in general, are widely used in the pharmaceutical industry for various applications, including the development of drugs.

Explanation

Urea derivatives are also utilized in the development of pesticides and herbicides, which are essential for crop protection and management.

Explanation

The chemical formula represents the composition of the compound, indicating the number of carbon (C), hydrogen (H), chlorine (Cl), nitrogen (N), and oxygen (O) atoms present in the molecule.

Explanation

The molecular weight is an important property that can influence the compound's physical and chemical behavior.

Explanation

The solubility of the compound in different solvents is an important factor to consider for its potential applications and handling.

Explanation

The stability of the compound under various conditions is crucial for its potential use in pharmaceuticals, pesticides, or herbicides. Further research is needed to determine its stability profile.

Structure

Contains a 3-chlorophenyl group and a 3-(phenylmethoxy)(2-pyridyl) group

Potential applications

Medicine and agriculture

Further research needed

Synthesis and properties

Pharmaceutical relevance

Commonly used in pharmaceuticals

Agricultural relevance

Commonly used in pesticides and herbicides

Molecular weight

Approximately 285.74 g/mol

Solubility

Unknown, but may vary depending on the solvent

Stability

Unknown, but may be influenced by factors such as temperature, pH, and exposure to light

Check Digit Verification of cas no

The CAS Registry Mumber 877459-37-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,7,4,5 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 877459-37:
(8*8)+(7*7)+(6*7)+(5*4)+(4*5)+(3*9)+(2*3)+(1*7)=235
235 % 10 = 5
So 877459-37-5 is a valid CAS Registry Number.

877459-37-5SDS

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 1-(3-chlorophenyl)-3-(3-phenylmethoxypyridin-2-yl)urea

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:877459-37-5 SDS

877459-37-5Downstream Products

877459-37-5Relevant academic research and scientific papers

Synthesis of carbamates and ureas using Zr(IV)-catalyzed exchange processes

Han, Chong,Porco Jr., John A.

, p. 1517 - 1520 (2007)

Equation presented Zirconium(IV)-catalyzed exchange processes have been developed to prepare both carbamates and ureas from dialkyl arbonates and carbamates employing 2-hydroxypyridine (HYP) and 4-methyl-2-hydroxyquinoline (MeHYQ) as catalytic additives, respectively A microwave acceleration effect was observed in Zr(IV)-catalyzed carbamate-urea exchange.

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