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1-(4-Methoxyphenyl)imidazoline-2-thione is a chemical compound that belongs to the imidazoline derivative class. It is characterized by a thione group attached to an imidazoline ring, with a methoxy group attached to the phenyl ring. 1-(4-METHOXYPHENYL)IMIDAZOLINE-2-THIONE is known for its potential pharmacological activities and its ability to act as a ligand in metal-catalyzed reactions, making it a versatile component in the synthesis of pharmaceuticals and agrochemicals.

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  • 17452-14-1 Structure
  • Basic information

    1. Product Name: 1-(4-METHOXYPHENYL)IMIDAZOLINE-2-THIONE
    2. Synonyms: 1-(4-METHOXYPHENYL)IMIDAZOLINE-2-THIONE;1-(4-Methoxyphenyl)-1,3-dihydro-2H-imidazole-2-thione;1-(4-Methoxyphenyl)-1H-iMidazole-2(3H)-thione
    3. CAS NO:17452-14-1
    4. Molecular Formula: C10H10N2OS
    5. Molecular Weight: 206.26
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 17452-14-1.mol
  • Chemical Properties

    1. Melting Point: 216-217°C
    2. Boiling Point: 336.6°Cat760mmHg
    3. Flash Point: 157.4°C
    4. Appearance: /
    5. Density: 1.32g/cm3
    6. Vapor Pressure: 0.000111mmHg at 25°C
    7. Refractive Index: 1.689
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. BRN: 155898
    11. CAS DataBase Reference: 1-(4-METHOXYPHENYL)IMIDAZOLINE-2-THIONE(CAS DataBase Reference)
    12. NIST Chemistry Reference: 1-(4-METHOXYPHENYL)IMIDAZOLINE-2-THIONE(17452-14-1)
    13. EPA Substance Registry System: 1-(4-METHOXYPHENYL)IMIDAZOLINE-2-THIONE(17452-14-1)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: N/A
    3. Safety Statements: 22-24/25
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 17452-14-1(Hazardous Substances Data)

17452-14-1 Usage

Uses

Used in Pharmaceutical Synthesis:
1-(4-Methoxyphenyl)imidazoline-2-thione is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to act as a ligand in metal-catalyzed reactions. This property allows for the creation of new drug molecules with improved therapeutic properties.
Used in Agrochemical Synthesis:
In the agrochemical industry, 1-(4-Methoxyphenyl)imidazoline-2-thione is utilized as a building block for the development of new agrochemicals. Its unique structure and reactivity contribute to the creation of effective compounds for pest control and crop protection.
Used in Antimicrobial Applications:
1-(4-Methoxyphenyl)imidazoline-2-thione has been investigated for its potential antimicrobial properties. It is used as an antimicrobial agent in various applications, such as in the development of new antibiotics or as a preservative in different products, to combat bacterial infections.
Used in Antifungal Applications:
1-(4-METHOXYPHENYL)IMIDAZOLINE-2-THIONE has also shown promise in antifungal research, making it a valuable asset in the development of new antifungal agents. It is used in the formulation of antifungal medications and treatments to address fungal infections in both medical and agricultural settings.

Check Digit Verification of cas no

The CAS Registry Mumber 17452-14-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,4,5 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17452-14:
(7*1)+(6*7)+(5*4)+(4*5)+(3*2)+(2*1)+(1*4)=101
101 % 10 = 1
So 17452-14-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H10N2OS/c1-13-9-4-2-8(3-5-9)12-7-6-11-10(12)14/h2-7H,1H3,(H,11,14)

17452-14-1 Well-known Company Product Price

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  • Alfa Aesar

  • (L12216)  1-(4-Methoxyphenyl)imidazoline-2-thione, 98%   

  • 17452-14-1

  • 1g

  • 401.0CNY

  • Detail
  • Alfa Aesar

  • (L12216)  1-(4-Methoxyphenyl)imidazoline-2-thione, 98%   

  • 17452-14-1

  • 5g

  • 1431.0CNY

  • Detail

17452-14-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-METHOXYPHENYL)IMIDAZOLINE-2-THIONE

1.2 Other means of identification

Product number -
Other names 1-(4-Methoxyphenyl)-1H-imidazole-2(3H)-thione

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:17452-14-1 SDS

17452-14-1Relevant articles and documents

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Paragraph 0017-0018, (2021/12/07)

The method comprises the following steps: suspending metal hydride in anhydrous THF, dropwise adding ring thiourea in the stirring process, stirring at room temperature after completion of stirring, stirring at room temperature, TLC monitoring reaction co

Synthesis and biological evaluation of imidazole thioacetanilides as novel non-nucleoside HIV-1 reverse transcriptase inhibitors

Zhan, Peng,Liu, Xinyong,Zhu, Junjie,Fang, Zengjun,Li, Zhenyu,Pannecouque, Christophe,Clercq, Erik De

experimental part, p. 5775 - 5781 (2009/12/28)

A series of 2-(1-aryl-1H-imidazol-2-ylthio)acetamide [imidazole thioacetanilide (ITA)] derivatives were synthesized and evaluated as potent inhibitors of human immunodeficiency virus type-1 (HIV-1). Among them, the most potent HIV-1 inhibitors were 4a5 (E

New bis(mercaptoimidazolyl)(pyrazolyl)borate ligands and their zinc complex chemistry

Shu, Mouhai,Walz, Rainer,Wu, Biao,Seebacher, Jan,Vahrenkamp, Heinrich

, p. 2502 - 2511 (2007/10/03)

Nine new tripodal NS2 ligands of the bis(mercaptoimidazolyl)(pyrazolyl)borate type with varying 3-R-mercaptoimidazolyl moieties were prepared as their potassium salts. Treatment with zinc salts yielded the complex types L·Zn-Cl, L·Zn-I, L·Zn-ONO2, L·Zn-OClO3 and [L·Zn(imidazole)]ClO4. Attempts at the formation of L·Zn-OH or cationic L·Zn complexes resulted in dismutation and formation of ZnL2 complexes. Hydrolytic destruction yielded one [OZn4(thiooimidazolate)6] complex. The ZnS2NO coordination which is present in the enzyme-substrate complex of alcohol dehydrogenase could be successfully modelled by an [L·Zn(C2H5OH)]+ complex. The L·Zn-X complexes showed very low catalytic activity in the dehydrogenation of 2-propanol or the hydrogenation of p-nitrobenzaldehyde. The new compounds were identified by a total of 12 structure determinations. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003.

DOPAMINE-BETA-HYDROXYLASE INHIBITORS

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2-(aminoalkylthio)imidazoles as dopamine-β-hydroxylase inhibitors

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