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2-(2-(Pyridin-2-yl)disulfanyl)ethanol, also known as DEDC, is a colorless liquid chemical compound with a molecular formula C8H9NOS2. It is characterized by a faint odor and is used as a thiol compound in various fields, including organic synthesis and pharmaceutical research. DEDC is a versatile reagent in chemical reactions, particularly in metal-catalyzed reactions, and is employed in the synthesis of pharmaceuticals and agrochemicals. Its ability to chelate metals makes it a potential candidate for the treatment of metal poisoning, while its antioxidant properties have shown promise in protecting cells from oxidative damage. Overall, 2-(2-(Pyridin-2-yl)disulfanyl)ethanol is a valuable and multifunctional chemical compound with diverse applications in chemistry and medicine.

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  • 111625-28-6 Structure
  • Basic information

    1. Product Name: 2-(2-(pyridin-2-yl)disulfanyl)ethanol
    2. Synonyms: 2-(2-(pyridin-2-yl)disulfanyl)ethanol;2-(Pyridin-2-yldisulfanyl)ethanol;2-(pyridin-2-yldisulfanyl)ethan-1-ol;S-2-pyridyl-S'-2-hydroxyethyl disulfide;Ethanol, 2-(2-pyridinyldithio)-
    3. CAS NO:111625-28-6
    4. Molecular Formula: C7H9NOS2
    5. Molecular Weight: 187.28246
    6. EINECS: -0
    7. Product Categories: N/A
    8. Mol File: 111625-28-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(2-(pyridin-2-yl)disulfanyl)ethanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(2-(pyridin-2-yl)disulfanyl)ethanol(111625-28-6)
    11. EPA Substance Registry System: 2-(2-(pyridin-2-yl)disulfanyl)ethanol(111625-28-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 111625-28-6(Hazardous Substances Data)

111625-28-6 Usage

Uses

Used in Organic Synthesis:
2-(2-(Pyridin-2-yl)disulfanyl)ethanol is used as a thiol compound in organic synthesis for its versatility in chemical reactions, including metal-catalyzed reactions. It aids in the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new and improved chemical compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-(2-(Pyridin-2-yl)disulfanyl)ethanol is used as a reagent in the synthesis of various pharmaceuticals. Its ability to chelate metals makes it a potential candidate for the treatment of metal poisoning, offering a novel approach to addressing this medical condition.
Used in Antioxidant Applications:
2-(2-(Pyridin-2-yl)disulfanyl)ethanol is used as an antioxidant in protecting cells from oxidative damage. Its potential in this area has shown promise, making it a valuable compound for further research and development in the field of antioxidants and cell protection.
Used in Metal Chelation Therapy:
In the medical industry, 2-(2-(Pyridin-2-yl)disulfanyl)ethanol is used as a potential treatment for metal poisoning due to its ability to chelate metals. This application offers a new avenue for the development of therapies to counteract the harmful effects of metal poisoning.

Check Digit Verification of cas no

The CAS Registry Mumber 111625-28-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,6,2 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 111625-28:
(8*1)+(7*1)+(6*1)+(5*6)+(4*2)+(3*5)+(2*2)+(1*8)=86
86 % 10 = 6
So 111625-28-6 is a valid CAS Registry Number.

111625-28-6SDS

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 S-2-pyridyl-S'-2-hydroxyethyl disulfide

1.2 Other means of identification

Product number -
Other names 2-(2-(pyridin-2-yl)disulfanyl)ethanol

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:111625-28-6 SDS

111625-28-6Relevant articles and documents

Photoinduced heterodisulfide metathesis for reagent-free synthesis of polymer nanoparticles

Li, Longyu,Song, Cunfeng,Jennings, Matthew,Thayumanavan

, p. 1425 - 1428 (2015)

Reagent-free synthetic methods are of great interest because of their simplicity and implications in green chemistry. We have taken advantage of photoinduced heterodisulfide metathesis to generate crosslinked polymer nanoparticles. The method of development and the mechanistic basis for the synthetic approach are outlined in this communication.

Nanoscale organization of thiol and arylsulfonic acid on silica leads to a highly active and selective bifunctional, heterogeneous catalyst

Margelefsky, Eric L.,Bendjeriou, Anissa,Zeidan, Ryan K.,Dufaud, Veronique,Davis, Mark E.

experimental part, p. 13442 - 13449 (2009/02/06)

Ordered mesoporous silicas functionalized with alkylsulfonic acid and thiol group pairs have been shown to catalyze the synthesis of bisphenols from the condensation of phenol and various ketones, with activity and selectivity highly dependent on the distance between the acid and thiol. Here, a new route to thiol/sulfonic acid paired catalysts is reported. A bis-silane precursor molecule containing both a disulfide and a sulfonate ester bond is grafted onto the surface of ordered mesoporous silica, SBA-15, followed by simultaneous disulfide reduction and sulfonate ester hydrolysis. The resulting catalyst, containing organized pairs of arylsulfonic acid and thiol groups, is significantly more active than the alkylsulfonic acid/thiol paired catalyst in the synthesis of bisphenol A and Z, and this increase in activity does not lead to a loss of regioselectivity. The paired catalyst has activity similar to that of a randomly bifunctionalized arylsulfonic acid/thiol catalyst in the bisphenol A reaction but exhibits greater activity and selectivity than the randomly bifunctionalized catalyst in the bisphenol Z reaction.

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