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1H-Imidazol-2-amine,4-(4-ethoxyphenyl)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76507-16-9

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76507-16-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76507-16-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,5,0 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 76507-16:
(7*7)+(6*6)+(5*5)+(4*0)+(3*7)+(2*1)+(1*6)=139
139 % 10 = 9
So 76507-16-9 is a valid CAS Registry Number.

76507-16-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-ethoxyphenyl)-2-aminoimidazole

1.2 Other means of identification

Product number -
Other names 4-(4-Ethoxy-phenyl)-1H-imidazol-2-ylamine

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:76507-16-9 SDS

76507-16-9Relevant academic research and scientific papers

Method for inhibiting advanced glycosylation of proteins using aminosubstituted imidazoles

-

, (2008/06/13)

The present invention relates to compositions and methods for inhibiting nonenzymatic cross-linking (protein aging), Accordingly, a composition is disclosed which comprises 2-aminoimidazoles capable of inhibiting the formation of advanced glycosylation endproducts of target proteins by reacting with the carbonyl moiety of the early glycosylation product of such target proteins formed by their initial glycosylation, The method comprises contacting the target protein with the composition, Both industrial and therapeutic applications for the invention are envisioned, as food spoilage and animal protein aging can be treated.

Synthesis and Halogenation of Some New 2-Amino-4-substituted Iminazoles and Their Possible Use as Pesticides

Nath, J. P.,Mahapatra, G. N.

, p. 526 - 528 (2007/10/02)

2-Amino-4-substituted iminazoles (1a-k) have been synthesised by condensing various ketones with guanidine using bromine as condensing agent in dry methanol.These have been halogenated to yield the corresponding 5-halogeno derivatives (II, III).Both halogenated and nonhalogenated iminazoles exhibit antifungal activity against Piricularia oryzae (Cav.) and antibacterial activity against the common pathogenic bacteria, Staphy. aureus and Esch. coli.Structure-activity relationship has also been discussed.

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