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2-Imidazolidinone, 4,5-dimethyl- is a chemical compound with the molecular formula C5H10N2O. It is a cyclic amine derivative, specifically a substituted imidazolidinone, which is a type of imidazole ring fused to a lactam. 2-Imidazolidinone, 4,5-dimethyl- is characterized by two methyl groups attached to the 4 and 5 positions of the imidazolidinone ring, which influences its chemical properties and reactivity. It is used in various applications, including as a building block in the synthesis of pharmaceuticals and other organic compounds, due to its unique structure and potential to form stable intermediates in chemical reactions.

3169-20-8

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3169-20-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3169-20-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,6 and 9 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3169-20:
(6*3)+(5*1)+(4*6)+(3*9)+(2*2)+(1*0)=78
78 % 10 = 8
So 3169-20-8 is a valid CAS Registry Number.

3169-20-8SDS

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 4,5-dimethylimidazolidin-2-one

1.2 Other means of identification

Product number -
Other names 4,5-dimethyl-imidazolidin-2-one

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:3169-20-8 SDS

3169-20-8Downstream Products

3169-20-8Relevant academic research and scientific papers

(Enantio)selective Hydrogen Autotransfer: Ruthenium-Catalyzed Synthesis of Oxazolidin-2-ones from Urea and Diols

Pe?a-López, Miguel,Neumann, Helfried,Beller, Matthias

, p. 7826 - 7830 (2016)

A novel strategy for the synthesis of oxazolidin-2-ones from vicinal diols and urea is described. In this heterocycle synthesis, two different C?O and C?N bonds are sequentially formed in a domino process consisting of nucleophilic substitution and alcohol amination. The use of readily available starting materials and the good atom economy render this process environmentally benign. While this transformation is already highly chemo- and regioselective, we also developed the first asymmetric version of this method using (R)-(+)-MeO-BIPHEP as the chiral ligand.

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