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(2-Chloroethyl)diMethylsulfoniuM iodide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 25059-70-5 Structure
  • Basic information

    1. Product Name: (2-Chloroethyl)diMethylsulfoniuM iodide
    2. Synonyms: (2-Chloroethyl)diMethylsulfoniuM iodide;(2-CHLOROETHYL)DIMETHYLSULFANIUM IODIDE
    3. CAS NO:25059-70-5
    4. Molecular Formula: C4H10ClS*I
    5. Molecular Weight: 252.54467
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 25059-70-5.mol
  • Chemical Properties

    1. Melting Point: 90-91 °C
    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-Chloroethyl)diMethylsulfoniuM iodide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2-Chloroethyl)diMethylsulfoniuM iodide(25059-70-5)
    11. EPA Substance Registry System: (2-Chloroethyl)diMethylsulfoniuM iodide(25059-70-5)
  • 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: 25059-70-5(Hazardous Substances Data)

25059-70-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25059-70-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,0,5 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 25059-70:
(7*2)+(6*5)+(5*0)+(4*5)+(3*9)+(2*7)+(1*0)=105
105 % 10 = 5
So 25059-70-5 is a valid CAS Registry Number.

25059-70-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloroethyl(dimethyl)sulfanium,iodide

1.2 Other means of identification

Product number -
Other names Chloroethyldimethylsulfonium iodide

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:25059-70-5 SDS

25059-70-5Relevant articles and documents

5-HT2C RECEPTOR AGONISTS AND COMPOSITIONS AND METHODS OF USE

-

Page/Page column 100, (2017/02/28)

Provided in some embodiments are compounds of Formula A, as defined herein, that modulate the activity of 5-HT2C receptor. Also provided in some embodiments are methods, such as, for weight management, inducing satiety, and decreasing food intake, and for

ALDOSTERONE SYNTHASE INHIBITORS

-

Page/Page column 48-49, (2016/06/28)

The present invention relates to compounds of the formulas (IA) and (IB) and pharmaceutically acceptable salts thereof, wherein A and R1 - R6, are as defined herein. The invention also relates to pharmaceutical compositions comprisin

CYCLOHEXANE-1,2'-NAPHTHALENE-1',2"-IMIDAZOLE COMPOUNDS AND THEIR USE AS BACE INHIBITORS

-

Page/Page column 28, (2014/01/09)

Cyclohexane-1,2'-naphthalene-1',2''-imidazole compounds, therapeutically acceptable salts thereof, processes for preparation thereof, therapeutic uses of such compounds for treating Aβ-related pathologies such as Down's syndrome, β-amyloid angiopathy, Alzheimer's disease, memory loss, attention deficit symptoms associated with Alzheimer's disease, neurodegeneration associated with diseases such as Alzheimer's disease or dementia including dementia of mixed vascular and degenerative origin, pre-senile dementia, senile dementia and dementia associated with Parkinson's disease, progressive supranuclear palsy or cortical basal degeneration, methods of therapy using such compounds, and pharmaceutical compositions containing such compounds.

Design and synthesis of violet odorants with bicyclo[6.4.0]dodecene and bicyclo[5.4.0]undecene skeletons

Kraft, Philip

, p. 695 - 703 (2007/10/03)

The Diels-Alder reaction of 1,2-bis(methylene)cyclooctane (13), 4- methylenespiro[2.7]decane (29), 4-methylenespiro[2.6]nonane (40) and 4- methylenespiro[2.7]dec-8-ene (46) with different α,β-unsaturated carbonyl compounds afforded various derivatives 16, 18, 20, 22, 24, 26, 32, 36, 38, 41, 42 and 47 of a molecular-modeled lead compound 9. These less flexible β- ionone-mimics with bicyclo[6.4.0]dodecene and bicyclo[5.4.0]undecene skeletons possess interesting fruity-woody-floral odor notes and provide insight into the structure-odor correlation of violet odorants. 5-(2- Methylcycloalk-1-en-1-yl)hex-3-en-2-ones (e.g. 35) were identified as byproducts of the Rh(I)-catalyzed reactions of the vinylcyclopropanes 29 and 40.

Reactions of 2-Chloroethyl sulfides: III. Mechanism of methanolysis of 2-Chloroethyl sulfides

Fomina,Vishnyakov,Glushkov

, p. 1282 - 1288 (2007/10/03)

The products and kinetics of methanolysis of 2-chloroethyl methyl sulfide, 2-chloroethyl 2-methoxyethyl sulfide, 2,2′-dichlorodiethyl sulfide, and 2-chloroethyl phenyl sulfide (at a concentration of 0.05-0.2 M) were studies by 13C NMR spectroscopy and gas-liquid chromatography. The rate of methanolysis decreases in the following series: methyl > methoxyethyl > 2-chloroethyl > phenyl. The amount of sulfonium dimers among the products decreases in the same series; the rate of dimerization of 2-chloroethyl methyl sulfide exceeds the rate of methanolysis. The reaction of 2-chloroethyl sulfides in methanol with a strong neutral nucleophile, thiourea, is of the second order. The rate constants of this reaction show a correlation with the constants σ* of substituents on the sulfur, which is similar to that found for the hydrolysis. This correlation indicates formation of intermediate ethylenesulfonium ion. Unlike the hydrolysis process, the rate-determining stage in the methanolysis is the reaction of ethylsulfonium ion with the nucleophile rather than ionization of 2-chloroethyl sulfide.

Synthesis of mitomycin and its analogs

-

, (2008/06/13)

The present invention relates to the synthesis of mitomycin and analogs thereof that are useful as anticancer antibiotics. The invention further relates to analogs of mitomycin, which can be prepared according to the methods of synthesis provided. The synthetic method of the invention provides for reacting a derivitized indole with a dialkylvinylsulfonium salt to yield a tricyclic skeleton having the precursors of the fourth ring in one step, followed by an oxidation step or steps to close the fourth ring and prepare mitomycin or a related compound.

2-CHLOROETHYL DIMETHYL SULFONIUM IODIDE.

Ruder, Suzanne M.,Ronald, Robert C.

, p. 5501 - 5504 (2007/10/02)

Ketones are readily spiroannelated by 2-chloroethyldimethyl sulfonium iodide 1 in the presence of t-butoxide anion in t-butanol.The procedure affords a simple one step spirocyclopropanation of ketones in good yields.

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