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CAS

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108122-14-1

(2-Iodoethyl)(Methyl)sulfane is a chemical compound formed by the combination of one molecule of ethyl iodide (iodoethane) and one molecule of methyl sulfane (methanethiol). Ethyl iodide is a colorless liquid with a strong, sweet odor, commonly used as a laboratory reagent in organic synthesis and as an alkylating agent. Methyl sulfane, a colorless gas with a strong, unpleasant odor, serves as a precursor to certain organosulfur compounds and as a reagent in organic synthesis. The resulting compound is potentially reactive and volatile, necessitating careful handling and adherence to proper safety protocols.

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  • 108122-14-1 Structure

  • Basic information

    1. Product Name: (2-iodoethyl)(Methyl)sulfane
    2. Synonyms: (2-iodoethyl)(Methyl)sulfane;1-iodo-2-(methylthio)ethane
    3. CAS NO:108122-14-1
    4. Molecular Formula: C3H7IS
    5. Molecular Weight: 202.05715
    6. EINECS: -0
    7. Product Categories: N/A
    8. Mol File: 108122-14-1.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-iodoethyl)(Methyl)sulfane(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2-iodoethyl)(Methyl)sulfane(108122-14-1)
    11. EPA Substance Registry System: (2-iodoethyl)(Methyl)sulfane(108122-14-1)

  • 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: 108122-14-1(Hazardous Substances Data)

108122-14-1 Usage

Uses

Used in Organic Synthesis:
(2-Iodoethyl)(Methyl)sulfane is used as a reagent in organic synthesis for its potential to participate in various chemical reactions due to its reactive nature.
Used in Laboratory Research:
As a compound with unique properties, (2-Iodoethyl)(Methyl)sulfane is used in laboratory research to explore its chemical behavior and potential applications in the development of new chemical processes or products.
Used in the Production of Organosulfur Compounds:
(2-Iodoethyl)(Methyl)sulfane is used as a precursor in the synthesis of specific organosulfur compounds, contributing to the advancement of sulfur chemistry and its applications.
Used in Alkylation Processes:
(2-Iodoethyl)(Methyl)sulfane is utilized as an alkylating agent in various chemical processes, where it can transfer an alkyl group to another molecule, altering its properties and function.

Check Digit Verification of cas no

The CAS Registry Mumber 108122-14-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,1,2 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 108122-14:
(8*1)+(7*0)+(6*8)+(5*1)+(4*2)+(3*2)+(2*1)+(1*4)=81
81 % 10 = 1
So 108122-14-1 is a valid CAS Registry Number.

108122-14-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-iodo-2-methylsulfanylethane

1.2 Other means of identification

Product number -
Other names 2-iodoethyl methyl sulfide

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:108122-14-1 SDS

108122-14-1Relevant articles and documents

O2-sulfonylethyl protected isopropylamine diazen-1-ium-1,2- diolates as nitroxyl (HNO) donors: Synthesis, β-elimination fragmentation, HNO release, positive inotropic properties, and blood pressure lowering studies

Huang, Zhangjian,Kaur, Jatinder,Bhardwaj, Atul,Alsaleh, Nasser,Reisz, Julie A.,DuMond, Jenna F.,King, S. Bruce,Seubert, John M.,Zhang, Yihua,Knaus, Edward E.

supporting information, p. 10262 - 10271 (2013/01/16)

New types of nonexplosive O2-sulfonylethyl protected (-CH 2CH2SO2R; R = OMe, NHOMe, NHOBn, Me) derivatives of isopropylamine diazen-1-ium-1,2-diolate (IPA/NO) (2-5) were developed that are designed to act as novel HNO donors. These compounds, with suitable half-lives (6.6-17.1 h) at pH 7.4, undergo a base-induced β-elimination reaction that releases a methyl vinyl sulfone product and the parent IPA/NO anion which subsequently preferentially releases HNO (46-61% range). Importantly, the O2-methylsulfonylethyl compound 5 exhibited a significant in vitro inotropic effect up to 283% of the baseline value and increased the rates of contraction and relaxation but did not induce a chronotropic effect. Furthermore, compound 5 (22.5 mg/kg po dose) provided a significant reduction in blood pressure up to 6 h after drug administration. All these data suggest that O2-sulfonylethyl protected derivatives of IPA/NO, which are efficient HNO donors, could have potential applications to treat cardiovascular disease(s) such as congestive heart failure.

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