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500167-99-7

1H-Imidazole,2-(ethenylthio)-1-methyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 500167-99-7 Structure

  • Basic information

    1. Product Name: 1H-Imidazole,2-(ethenylthio)-1-methyl-(9CI)
    2. Synonyms: 1H-Imidazole,2-(ethenylthio)-1-methyl-(9CI);2-(ethenylthio)-1-methyl-1H-Imidazole
    3. CAS NO:500167-99-7
    4. Molecular Formula: C6H8N2S
    5. Molecular Weight: 140.209
    6. EINECS: N/A
    7. Product Categories: AMINETERTIARY
    8. Mol File: 500167-99-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 237.3 °C at 760 mmHg
    3. Flash Point: 97.3 °C
    4. Appearance: /
    5. Density: 1.14 g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. Water Solubility: at 25 deg C (mg/L): 3390
    10. CAS DataBase Reference: 1H-Imidazole,2-(ethenylthio)-1-methyl-(9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1H-Imidazole,2-(ethenylthio)-1-methyl-(9CI)(500167-99-7)
    12. EPA Substance Registry System: 1H-Imidazole,2-(ethenylthio)-1-methyl-(9CI)(500167-99-7)

  • 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: 500167-99-7(Hazardous Substances Data)

500167-99-7 Usage

Structure

A derivative of imidazole with a methyl group attached to the nitrogen atom and an ethenylthio group attached to the second carbon atom.

Usage

Commonly used in organic synthesis, as a ligand in coordination chemistry, and as a precursor in the pharmaceutical industry.

Biological activities

Potential antimicrobial, anticancer, and anti-inflammatory properties.

Research status

Has been studied for its potential biological activities, but further research is needed to fully understand its potential applications and effects.

Check Digit Verification of cas no

The CAS Registry Mumber 500167-99-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,0,1,6 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 500167-99:
(8*5)+(7*0)+(6*0)+(5*1)+(4*6)+(3*7)+(2*9)+(1*9)=117
117 % 10 = 7
So 500167-99-7 is a valid CAS Registry Number.

500167-99-7SDS

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 1H-Imidazole,2-(ethenylthio)-1-methyl-(9CI)

1.2 Other means of identification

Product number -
Other names -

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:500167-99-7 SDS

500167-99-7Downstream Products

500167-99-7Relevant articles and documents

Calcium carbide as a convenient acetylene source in the synthesis of unsaturated sulfides, promising functionalized monomers

Rodygin, Konstantin S.,Kostin, Anton A.,Ananikov, Valentine P.

, p. 415 - 416 (2015/12/30)

Calcium carbide was studied as a useful solid-state reagent to incorporate acetylene unit into synthetic procedures. Atom-economic thiol-yne click reaction was successfully performed with single and double additions. Heterocyclic thiols and aliphatic dithiols reacted with acetylene generated in situ from calcium carbide to afford corresponding vinyl sulfides and bis(thiovinyl)ethers in good to high yields.

Synthesis of N- and S-vinyl derivatives of heteroaromatic compounds using phase-transfer catalysis

Abele,Dzenitis,Rubina,Lukevics

, p. 682 - 685 (2007/10/03)

A method has been developed for the synthesis of N- and S-vinyl derivatives of heteroaromatic compounds from NH heterocycles or their thiols in the phase-transfer catalytic system ClCH2CH2Br-KOH (s)-18-crown-6-toluene. It is shown that it is possible to prepare N,S-divinyl derivatives of 3-mercaptoindole and 2-mercaptobenzimidazole.

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