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1H-Imidazol-2-amine, 4,5-dihydro-N-(4-methylphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

4794-82-5

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4794-82-5 Usage

Class of compound

Imidazole derivative

Structure

1H-Imidazol-2-amine, 4,5-dihydro with a substituted amine group and a 4-methylphenyl group

Usage

Synthesis of pharmaceuticals

Biological activity

Potential biological activity

Importance

Building block in the development of medicinal and chemical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 4794-82-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,9 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4794-82:
(6*4)+(5*7)+(4*9)+(3*4)+(2*8)+(1*2)=125
125 % 10 = 5
So 4794-82-5 is a valid CAS Registry Number.

4794-82-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-methylphenyl)-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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4794-82-5 SDS

4794-82-5Downstream Products

4794-82-5Relevant academic research and scientific papers

Ti-amide catalyzed synthesis of cyclic guanidines from di-/triamines and carbodiimides

Shen, Hao,Wang, Yang,Xie, Zuowei

supporting information; experimental part, p. 4562 - 4565 (2011/10/12)

A titanacarborane monoamide catalyzed, one-step synthesis of mono/bicyclic guanidines from commercially available di/triamines and carbodiimides is reported. The reaction mechanism is also proposed.

One-pot synthesis of iminoimidazolines under microwave irradiation in solvent-free conditions

Servi, Sueleyman,Genc, Murat

, p. 3173 - 3179 (2008/02/12)

Substituted iminoimidazolines were synthesized from a one-pot reaction of aromatic or hetero-aromatic amines with imidazolidine-2-thione under solvent-free conditions using microwave irradiation with good to excellent yields. Copyright Taylor & Francis Group, LLC.

The preparation of 1,2,3-trisubstituted guanidines

Katritzky, Alan R.,Khashab, Niveen M.,Bobrov, Sergey

, p. 1664 - 1675 (2007/10/03)

An operationally straightforward and efficient benzotriazole-based method for the guanylation of diverse amines by use of the new reagent classes (bis-benzotriazol-1-yl-methylene)amines 13a-13f and benzotriazole-1- carboxamidines 17a-17i is described. The preparation is described for a variety of both acyclic and cyclic 1,2,3-trisubstituted guanidines in high yields.

Microwave-assisted from synthesis of 2-arylamino-2-imidazolines on a solid support

Genc, Murat,Servi, Sueleyman

, p. 142 - 147 (2007/10/03)

An efficient synthesis of 2-arylamino-2-imidazolines from dimethyl N-aryldithioimidocarbonates and ethylenediamine on solid support under microwave irradiation has been developed. The reaction time has been reduced from hours to minutes with improved yiel

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