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N-(2,4,6-Trimethylphenyl)-2-imidazoline-2-amine is a chemical compound with the molecular formula C12H18N2. It is a derivative of imidazoline, a heterocyclic amine with a five-membered ring containing two nitrogen atoms. This specific compound features a 2,4,6-trimethylphenyl group attached to the nitrogen atom at position 1 of the imidazoline ring, and an amino group at position 2. It is known for its potential applications in pharmaceuticals and as a precursor in the synthesis of various organic compounds. The compound is characterized by its unique structure, which may contribute to its biological activity and reactivity in chemical reactions.

4201-40-5

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4201-40-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4201-40-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,0 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4201-40:
(6*4)+(5*2)+(4*0)+(3*1)+(2*4)+(1*0)=45
45 % 10 = 5
So 4201-40-5 is a valid CAS Registry Number.

4201-40-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2,4,6-trimethylphenyl)-4,5-dihydro-1H-imidazol-2-amine

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

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More Details:4201-40-5 SDS

4201-40-5Downstream Products

4201-40-5Relevant academic research and scientific papers

Three-dimensional common-feature hypotheses for octopamine agonist 2-(arylimino)imidazolidines

Hirashima, Akinori,Morimoto, Masako,Kuwano, Eiichi,Taniguchi, Eiji,Eto, Morifusa

, p. 117 - 123 (2007/10/03)

Three-dimensional pharmacophore hypotheses were built from a set of 10 octopamine (OA) agonist 2-(Arylimino)imidazolidines (AIIs), 2-(Arylimino)thiazolidines (AITs) and 2-(Arylimino)oxazolidines (AIOs). Among the 10 common-featured models generated by program Catalyst/HipHop, a hypothesis including a ring aromatic (RA), a positive ionizable (PI) and three hydrophobic aliphatic (HpA1) features was considered to be important in evaluating the OA-agonist activity. Active OA agonist 2,6-Et2 AII mapped well onto all the RA, PI and HpAl features of the hypothesis. On the other hand, less active compounds were shown to be difficult to achieve the energetically favorable conformation which is found in the active molecules in order to fit the 3-D common-feature pharmacophore models. Taken together, 2,6-Et2-Ph and foramidine structures are important as OA agonists. The present studies on OA agonists demonstrate that a RA, a PI and three HpAl sites located on the molecule seem to be essential for OA-agonist activity. Copyright

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