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4-(2-aminoethyl)-2,6-diiodo-phenol is an organic compound with the molecular formula C8H9IN2O. It is a derivative of phenol, characterized by the presence of two iodine atoms at the 2nd and 6th positions, an aminoethyl group attached to the 4th position, and a hydroxyl group. 4-(2-aminoethyl)-2,6-diiodo-phenol is known for its potential applications in the synthesis of pharmaceuticals and other chemical products. It is a white crystalline solid that is soluble in organic solvents. Due to the presence of iodine atoms, it may exhibit unique chemical properties and reactivity, making it a subject of interest in various chemical research and industrial applications.

370-00-3

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370-00-3 Usage

Structure

Consists of a phenolic ring with two iodine atoms attached and a side chain containing an ethylamine group

Synthesis

Commonly used as a precursor in the synthesis of various pharmaceuticals and organic compounds

Biological Activities

Antioxidant: Exhibits antioxidant properties, potentially useful in combating oxidative stress-related diseases
Antimicrobial: Displays antimicrobial activity, suggesting potential as an antibacterial or antifungal agent
Anti-inflammatory: Shows anti-inflammatory properties, indicating potential in treating inflammatory conditions

Medical Applications

Valuable building block for the development of new drugs and medical treatments due to its structure and biological activities

Chemical Reactivity

Its unique properties and reactivity make it a key component in the field of organic chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 370-00-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,7 and 0 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 370-00:
(5*3)+(4*7)+(3*0)+(2*0)+(1*0)=43
43 % 10 = 3
So 370-00-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H9I2NO/c9-6-3-5(1-2-11)4-7(10)8(6)12/h3-4,12H,1-2,11H2

370-00-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-aminoethyl)-2,6-diiodophenol

1.2 Other means of identification

Product number -
Other names 3.5-Dijod-tyramin

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:370-00-3 SDS

370-00-3Relevant academic research and scientific papers

Anti-Parasite Activity of Novel 3,5-Diiodophenethyl-benzamides

Restrepo, Manuel Pastrana,Surmay, Verónica Surmay,Jaramillo, Elkin Galeano,Restrepo, Sara Robledo

, p. 116 - 123 (2018/12/13)

Novel iodotyramides with para-substituted benzoic acids were synthesized via electrophilic aromatic substitutions and amide coupling via N,N'-diisopropylcarbodiimide (DIC) in dimethylformamide (DMF). All derivatives were in vitro screened against U-937 ma

Determination of serum biotinidase activity with biotinyl derivatives of iodotyramines as substrates

Evangelatos,Kakabakos,Evangelatos,Ithakissios

, p. 1228 - 1231 (2007/10/02)

We synthesized biotinylated mono- and di-iodotyramine and their radioactive counterparts and used these substances as substrates to estimate serum biotinidase activity in a radioassay system. The K(m) values determined for mono- and di-iodobiotinyl derivatives were 15.8 and 25.9 μM, respectively, whereas, the maximum velocities of the enzymatic reaction were 27.0 and 8.7 nmol · min-1 · mL-1, respectively. Both substrates competed with biocytin for the same active site of the enzyme and the K(i) values were 7.30 and 9.56 μM for the mono- and di-iodinated substrate, respectively. Higher assay sensitivity was obtained using [125I]biotinyl- monoiodotyramine as substrate, and the values obtained were directly related with those determined with the well-established colorimetric method (r = 0.9377, n = 31). However, for routine use, the assay may be accomplished by diluting the radiotracer with biocytin instead of its 'cold' counterpart, because it is a commercially available reagent. The values obtained in this case were very well correlated with those determined by the colorimetric assay as well (r = 0.9289, n = 31).

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