structure of Thiourea, (6-chloro-3-pyridinyl)-

Thiourea, (6-chloro-3-pyridinyl)-

CAS No.: 125117-97-7
M. Wt: 187.65000
M. Fa: C6H6ClN3S
InChI Key: KQNRFXLAUHMUSH-UHFFFAOYSA-N

Names and Identifiers of Thiourea, (6-chloro-3-pyridinyl)-

CAS Number

125117-97-7

MDL Number

MFCD15525455

IUPAC Name

(6-chloropyridin-3-yl)thiourea

InChI

InChI=1S/C6H6ClN3S/c7-5-2-1-4(3-9-5)10-6(8)11/h1-3H,(H3,8,10,11)

InChIKey

KQNRFXLAUHMUSH-UHFFFAOYSA-N

Canonical SMILES

NC(=S)NC1=CC=C(Cl)N=C1

UNSPSC Code

12352100

Physical and chemical properties of Thiourea, (6-chloro-3-pyridinyl)-

Exact Mass

186.99700

H Bond Acceptors

1

H Bond Donors

2

LogP

2.18420

Molecular Formula

C6H6ClN3S

Molecular Weight

187.65000

PSA

87.57000

Safety Information of Thiourea, (6-chloro-3-pyridinyl)-

Pictograms

Signal Word

Warning

Safety Data Sheet

Supports customized editing of SDS information and downloading in PDF documents.

Applications of Thiourea, (6-chloro-3-pyridinyl)-

Of Thiourea Derivatives: Detailed Review" class="citation ml-xs inline" data-state="closed" href="https://www.mdpi.com/2624-8549/6/3/25" rel="nofollow noopener" target="_blank"> .
  • Material science: Thiourea derivatives are utilized in the synthesis of polymers and other materials due to their unique chemical properties.
  • Interaction Studies of Thiourea, (6-chloro-3-pyridinyl)-

    Studies on (6-Chloropyridin-3-yl)thiourea interactions focus on:

    • Binding affinity with proteins: Research has shown that this compound can interact with specific enzymes and receptors, influencing their activity.
    • Complex formation with metals: Its ability to form stable complexes with transition metals has been investigated for potential catalytic applications.

    Biological Activity of Thiourea, (6-chloro-3-pyridinyl)-

    This compound exhibits significant biological activities, including:

    • Antimicrobial properties: Studies have shown that (6-Chloropyridin-3-yl)thiourea demonstrates inhibitory effects against various bacterial strains, including Staphylococcus aureus and Escherichia coli .
    • Antitumor activity: It has been evaluated for its potential as an antitumor agent, with some derivatives showing promising results against solid tumors.
    • Anti-inflammatory effects: Certain derivatives of thiourea compounds have been noted for their ability to inhibit pro-inflammatory cytokines, suggesting potential therapeutic applications in inflammatory diseases

      Physical sample testing spectrum (NMR) of Thiourea, (6-chloro-3-pyridinyl)-

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