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Phenol, 2-[1-(1H-imidazol-1-yl)-2-(methylthio)ethenyl]is a chemical compound that features a phenol molecule with a 1-(1H-imidazol-1-yl)-2-(methylthio)ethenyl group attached. Phenol, 2-[1-(1H-imidazol-1-yl)-2-(methylthio)ethenyl]is distinguished by the presence of an imidazole group, which is known for its ability to bind with proteins and enzymes, and a methylthio group that may influence its reactivity and pharmacological profile. Its unique structure positions it for potential applications in pharmaceuticals and biological research, particularly in cancer treatment and anti-inflammatory drug development.

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  • 138206-46-9 Structure
  • Basic information

    1. Product Name: Phenol, 2-[1-(1H-imidazol-1-yl)-2-(methylthio)ethenyl]-
    2. Synonyms: Phenol, 2-[1-(1H-imidazol-1-yl)-2-(methylthio)ethenyl]-
    3. CAS NO:138206-46-9
    4. Molecular Formula: C12H12N2OS
    5. Molecular Weight: 232.30148
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 138206-46-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 438.4±55.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.19±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 9.43±0.30(Predicted)
    10. CAS DataBase Reference: Phenol, 2-[1-(1H-imidazol-1-yl)-2-(methylthio)ethenyl]-(CAS DataBase Reference)
    11. NIST Chemistry Reference: Phenol, 2-[1-(1H-imidazol-1-yl)-2-(methylthio)ethenyl]-(138206-46-9)
    12. EPA Substance Registry System: Phenol, 2-[1-(1H-imidazol-1-yl)-2-(methylthio)ethenyl]-(138206-46-9)
  • 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: 138206-46-9(Hazardous Substances Data)

138206-46-9 Usage

Uses

Used in Pharmaceutical Industry:
Phenol, 2-[1-(1H-imidazol-1-yl)-2-(methylthio)ethenyl]is used as a potential candidate in drug design and development for its ability to interact with various proteins and enzymes, which is crucial in the creation of new therapeutic agents.
Used in Cancer Treatment Research:
In the field of oncology, this compound is being explored for its potential role in cancer treatment, given its capacity to bind with biological targets that may be implicated in cancer progression and cell growth.
Used in Anti-Inflammatory Drug Development:
Phenol, 2-[1-(1H-imidazol-1-yl)-2-(methylthio)ethenyl]is also considered for the development of anti-inflammatory drugs, where its interaction with specific biological targets could help in managing inflammation and related conditions.
Used in Biological Research:
Phenol, 2-[1-(1H-imidazol-1-yl)-2-(methylthio)ethenyl]serves as a valuable tool in biological research, aiding scientists in understanding the mechanisms of action and potential therapeutic effects of similar chemical structures on various biological systems.

Check Digit Verification of cas no

The CAS Registry Mumber 138206-46-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,2,0 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 138206-46:
(8*1)+(7*3)+(6*8)+(5*2)+(4*0)+(3*6)+(2*4)+(1*6)=119
119 % 10 = 9
So 138206-46-9 is a valid CAS Registry Number.

138206-46-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-1-[1-(2-Hydroxyphenyl)-2-(methylthio)ethenyl]-1H-imidazole

1.2 Other means of identification

Product number -
Other names (E)-1-[1-(2-Hydroxyphenyl)-2-(methylthio)ethenyl]-1H-imidazole

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:138206-46-9 SDS

138206-46-9Relevant articles and documents

Neticonazole hydrochloride preparation method

-

, (2018/04/01)

The invention discloses a neticonazole hydrochloride preparation method, which comprises: carrying out an acylation reaction on imidazole and o-hydroxybenzoic acid, carrying out a wittig reaction on the product of the acylation reaction and 1-halogenated dimethyl sulfide, carrying out a reaction on the product of the wittig reaction and 1-halogenated pentane in an inorganic alkali, and salifying the product of the reaction and hydrochloric acid to obtain the neticonazole hydrochloride. According to the present invention, the method can avoid the use of the methanethiol and thionyl chloride, has characteristics of environmental protection, mild reaction condition, simple operation, simple post-treatment and high product purity, and is suitable for industrial production.

Synthesis and antifungal activities of a series of (1,2-disubstituted vinyl)imidazoles

Ogawa,Matsuda,Eto,Asaoka,Kuraishi,Iwasa,Nakashima,Yamaguchi

, p. 2301 - 2307 (2007/10/02)

A series of vinylimidazoles containing a hetero atom such as sulfur or oxygen at a β-position of the vinyl group was prepared and the antifungal activities were tested. It was found that sulfur-substituted derivatives such as (E)-1-[2-(methylthio)-1-[2-(p

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