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(3-METHOXY-PROPYL)-THIOUREA, with the molecular formula C6H14N2OS, is an organosulfur derivative and a member of the thiourea family. It is known for its high solubility in water and its ability to interact with metal ions, making it a versatile chemical compound for various industrial applications.

66892-33-9

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66892-33-9 Usage

Uses

Used in Chemical Industry:
(3-METHOXY-PROPYL)-THIOUREA is used as a corrosion inhibitor to protect metal surfaces from corrosion and extend the life of equipment.
(3-METHOXY-PROPYL)-THIOUREA is used as a polymerization accelerator to speed up the process of polymer formation, improving efficiency in the production of plastics and rubber.
Used in Pharmaceutical Industry:
(3-METHOXY-PROPYL)-THIOUREA is used as a chemical intermediate in the production of pharmaceuticals, contributing to the synthesis of various medicinal compounds.
Used in Pesticide Industry:
(3-METHOXY-PROPYL)-THIOUREA is used as a chemical intermediate in the production of pesticides, aiding in the development of effective crop protection agents.
Used in Organic Synthesis:
(3-METHOXY-PROPYL)-THIOUREA is used as a reagent in organic synthesis, facilitating the creation of a range of organic compounds for research and industrial purposes.
Used in Rubber and Plastics Production:
(3-METHOXY-PROPYL)-THIOUREA is used as a component in the production of rubber and plastics, enhancing the properties and performance of these materials.
It is important to handle (3-METHOXY-PROPYL)-THIOUREA with care, as it can be harmful if ingested or inhaled, and can cause irritation to the skin and eyes.

Check Digit Verification of cas no

The CAS Registry Mumber 66892-33-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,8,9 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 66892-33:
(7*6)+(6*6)+(5*8)+(4*9)+(3*2)+(2*3)+(1*3)=169
169 % 10 = 9
So 66892-33-9 is a valid CAS Registry Number.

66892-33-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methoxypropylthiourea

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:66892-33-9 SDS

66892-33-9Relevant academic research and scientific papers

Substituted 5,5′-diphenyl-2-thioxoimidazolidin-4-one as CB 1 cannabinoid receptor ligands: Synthesis and pharmacological evaluation

Muccioli, Giulio G.,Martin, Diana,Scriba, Gerhard K. E.,Poppitz, Wolfgang,Poupaert, Jacques H.,Wouters, Johan,Lambert, Didier M.

, p. 2509 - 2517 (2007/10/03)

A set of 30 substituted 5,5′-diphenyl-2-thioxoimidazolidin-4-one (thiohydantoins) derivatives was synthesized, and their affinity for the human CB1 cannabinoid receptor has been evaluated. These compounds are derived from the previously described cannabinoid ligands 5,5′- diphenylimidazolidine-2,4-dione (hydantoins). The replacement of the oxygen by a sulfur leads to an increase of the affinity while the function-i.e., inverse agonism-determined by [35S]-GTPγS experiments remains unaffected. Finally, to evaluate the molecular parameters that could influence the affinity of the thiohydantoins, molecular electrostatic potential as well as lipophilicity calculations were undertaken on representative thiohydantoins and hydantoins derivatives. In conclusion, 5,5′-bis-(4-iodophenyl)-3-butyl-2- thioxoimidazolidin-4-one (31) and 3-allyl-5,5′-bis(4-bromophenyl)-2- thioxoimidazolidin-4-one (32) possess the highest affinity for the CB 1 cannabinoid receptor described to date for the hydantoin and thiohydantoins series when compared in a same bioassay.

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