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1-(3-chlorophenyl)-3-(3-fluoro-4-methylphenyl)urea is a chemical compound with the molecular formula C14H11ClFN2O. It is a derivative of urea, featuring a 3-chlorophenyl group at the 1-position and a 3-fluoro-4-methylphenyl group at the 3-position. 1-(3-chlorophenyl)-3-(3-fluoro-4-methylphenyl)urea is an example of a substituted urea, which can have various applications in the field of chemistry, such as in the synthesis of pharmaceuticals or agrochemicals. The presence of both a chlorine atom and a fluorine atom in the molecule can influence its reactivity and physical properties, making it a potentially interesting candidate for further study and development.

5636-59-9

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5636-59-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5636-59-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,3 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5636-59:
(6*5)+(5*6)+(4*3)+(3*6)+(2*5)+(1*9)=109
109 % 10 = 9
So 5636-59-9 is a valid CAS Registry Number.

5636-59-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-chlorophenyl)-3-(3-fluoro-4-methylphenyl)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

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More Details:5636-59-9 SDS

5636-59-9Downstream Products

5636-59-9Relevant academic research and scientific papers

The reaction of dialkoxytitanacyclopropanes and dialkoxytitanacyclopropenes with carbon dioxide

Six, Yvan

, p. 1159 - 1160 (2007/10/03)

Dialkoxytitanacyclopropanes and dialkoxytitanacyclopropenes react with one molecule of carbon dioxide to afford diversely substituted carboxylic acids after hydrolysis.

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