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3H-1,2,4-Triazole-3-thione,4-ethyl-2,4-dihydro-5-(2-pyridinyl)-(9CI) is a heterocyclic chemical compound belonging to the class of triazole derivatives. It features a five-membered ring structure composed of three nitrogen atoms and two carbon atoms, with an additional ethyl and pyridinyl group attached. This versatile compound is known for its biological activity and is widely utilized in the synthesis of pharmaceuticals and agricultural chemicals.

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  • 438231-11-9 Structure
  • Basic information

    1. Product Name: 3H-1,2,4-Triazole-3-thione,4-ethyl-2,4-dihydro-5-(2-pyridinyl)-(9CI)
    2. Synonyms: 4-ethyl-5-(2-pyridyl)-2H-1,2,4-triazole-3-thione;4-ethyl-5-pyridin-2-yl-2H-1,2,4-triazole-3-thione;EU-0083273;ST5213630;3H-1,2,4-Triazole-3-thione,4-ethyl-2,4-dihydro-5-(2-pyridinyl)-(9CI);Albb-003360;4-ethyl-5-pyridin-2-yl-4H-1,2,4-triazole-3-thiol(SALTDATA: FREE)
    3. CAS NO:438231-11-9
    4. Molecular Formula: C9H10N4S
    5. Molecular Weight: 206.272
    6. EINECS: N/A
    7. Product Categories: ETHYL
    8. Mol File: 438231-11-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 309°C at 760 mmHg
    3. Flash Point: 140.7°C
    4. Appearance: /
    5. Density: 1.34g/cm3
    6. Vapor Pressure: 0.000656mmHg at 25°C
    7. Refractive Index: 1.699
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 3H-1,2,4-Triazole-3-thione,4-ethyl-2,4-dihydro-5-(2-pyridinyl)-(9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3H-1,2,4-Triazole-3-thione,4-ethyl-2,4-dihydro-5-(2-pyridinyl)-(9CI)(438231-11-9)
    12. EPA Substance Registry System: 3H-1,2,4-Triazole-3-thione,4-ethyl-2,4-dihydro-5-(2-pyridinyl)-(9CI)(438231-11-9)
  • 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: 438231-11-9(Hazardous Substances Data)

438231-11-9 Usage

Uses

Used in Pharmaceutical Industry:
3H-1,2,4-Triazole-3-thione,4-ethyl-2,4-dihydro-5-(2-pyridinyl)-(9CI) is used as an intermediate in the synthesis of various pharmaceuticals for its potential antifungal, antibacterial, and antiviral properties. Its unique structure allows it to be a promising candidate for the development of new drugs targeting a range of infectious diseases.
Used in Agricultural Chemical Industry:
In the agricultural sector, 3H-1,2,4-Triazole-3-thione,4-ethyl-2,4-dihydro-5-(2-pyridinyl)-(9CI) serves as a key component in the production of agrochemicals. Its biological activity makes it suitable for use in the development of fungicides, bactericides, and抗病毒 agents to protect crops and enhance agricultural productivity.
Used as a Corrosion Inhibitor:
3H-1,2,4-Triazole-3-thione,4-ethyl-2,4-dihydro-5-(2-pyridinyl)-(9CI) has been studied for its potential application as a corrosion inhibitor. Its ability to form protective films on metal surfaces can help prevent corrosion, making it a valuable compound in industries such as oil and gas, where equipment protection is crucial.
Used in Coordination Chemistry:
As a ligand in coordination chemistry, 3H-1,2,4-Triazole-3-thione,4-ethyl-2,4-dihydro-5-(2-pyridinyl)-(9CI) plays a significant role in the formation of coordination compounds. Its unique structure allows it to bind with metal ions, creating complexes with potential applications in catalysis, sensing, and materials science.
Overall, 3H-1,2,4-Triazole-3-thione,4-ethyl-2,4-dihydro-5-(2-pyridinyl)-(9CI) is a multifaceted compound with a broad spectrum of potential applications across various industries, particularly in the development of pharmaceuticals and agricultural chemicals, as well as in corrosion inhibition and coordination chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 438231-11-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,8,2,3 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 438231-11:
(8*4)+(7*3)+(6*8)+(5*2)+(4*3)+(3*1)+(2*1)+(1*1)=129
129 % 10 = 9
So 438231-11-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H10N4S/c1-2-13-8(11-12-9(13)14)7-5-3-4-6-10-7/h3-6H,2H2,1H3,(H,12,14)

438231-11-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-ethyl-3-pyridin-2-yl-1H-1,2,4-triazole-5-thione

1.2 Other means of identification

Product number -
Other names 4-ethyl-5-pyridin-2-yl-4H-1,2,4-triazole-3-thiol

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:438231-11-9 SDS

438231-11-9Downstream Products

438231-11-9Relevant articles and documents

Narrow SAR in odorant sensing Orco receptor agonists

Romaine, Ian M.,Taylor, Robert W.,Saidu, Samsudeen P.,Kim, Kwangho,Sulikowski, Gary A.,Zwiebel, Laurence J.,Waterson, Alex G.

, p. 2613 - 2616 (2015/02/19)

The systematic exploration of a series of triazole-based agonists of the cation channel insect odorant receptor is reported. The structure-activity relationships of independent sections of the molecules are examined. Very small changes to the compound structure were found to exert a large impact on compound activity. Optimal substitutions were combined using a 'mix-and-match' strategy to produce best-in-class compounds that are capable of potently agonizing odorant receptor activity and may form the basis for the identification of a new mode of insect behavior modification.

Narrow SAR in odorant sensing Orco receptor agonists

Romaine, Ian M.,Taylor, Robert W.,Saidu, Samsudeen P.,Kim, Kwangho,Sulikowski, Gary A.,Zwiebel, Laurence J.,Waterson, Alex G.

, p. 2613 - 2616 (2014/06/09)

The systematic exploration of a series of triazole-based agonists of the cation channel insect odorant receptor is reported. The structure-activity relationships of independent sections of the molecules are examined. Very small changes to the compound structure were found to exert a large impact on compound activity. Optimal substitutions were combined using a 'mix-and-match' strategy to produce best-in-class compounds that are capable of potently agonizing odorant receptor activity and may form the basis for the identification of a new mode of insect behavior modification.

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