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Urea, N-cyclohexyl-N'-ethyl-, also known as Ethylcyclohexylurea (Ethyl-CHU), is an organic compound with the chemical formula C9H18N2O. It is a white crystalline solid that is soluble in water and various organic solvents. Ethylcyclohexylurea is primarily used as a corrosion inhibitor in various industrial applications, such as oil and gas pipelines, water treatment systems, and cooling towers. It works by forming a protective film on metal surfaces, preventing the formation of rust and other types of corrosion. Additionally, it has been used as a flame retardant in plastics and textiles, as well as a stabilizer in various chemical formulations. Ethylcyclohexylurea is considered to be a low-toxicity compound, but it is still important to handle it with care and follow proper safety guidelines during its use.

36102-06-4

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36102-06-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36102-06-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,1,0 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 36102-06:
(7*3)+(6*6)+(5*1)+(4*0)+(3*2)+(2*0)+(1*6)=74
74 % 10 = 4
So 36102-06-4 is a valid CAS Registry Number.

36102-06-4SDS

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 1-cyclohexyl-3-ethylurea

1.2 Other means of identification

Product number -
Other names N-Cyclohexyl-N'-aethyl-harnstoff

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:36102-06-4 SDS

36102-06-4Relevant academic research and scientific papers

Oximes as reusable templates for the synthesis of ureas and carbamates by an: In situ generation of carbamoyl oximes

Senadi, Gopal Chandru,Mutra, Mohana Reddy,Lu, Ting-Yi,Wang, Jeh-Jeng

supporting information, p. 4272 - 4277 (2017/09/28)

Oximes have been identified as reusable templates for the synthesis of ureas and carbamates by an in situ generation of carbamoyl oximes under metal-free conditions. The recovered oxime has been utilised for three trials in the synthesis of urea derivatives without any loss in the yield and efficiency. In addition, this template approach could override the usage of hazardous and less stable isocyanates as substrates.

A New Convenient Method for the Synthesis of Symmetrical and Unsymmetrical N,N'-Disubstituted Ureas

Izdebski, Jan,Pawlak, Danuta

, p. 423 - 425 (2007/10/02)

A new method is described for the preparation of symmetrically and unsymmetrically disubstituted ureas by aminolysis of bis(4-nitrophenyl) carbonate.The second substitution is slower than the first one, and it is possible to isolate monosubstituted intermediates when equimolar amounts of substrates are used.The reaction of the intermediates with different amines give unsymmetrical derivatives of urea.

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