structure of Thiophene-2-carboximidamide

Thiophene-2-carboximidamide

CAS No.: 54610-75-2
M. Wt: 126.18000
M. Fa: C5H6N2S
InChI Key: QSELGEUCFNFITD-UHFFFAOYSA-N

Names and Identifiers of Thiophene-2-carboximidamide

CAS Number

54610-75-2

MDL Number

MFCD00939263

IUPAC Name

thiophene-2-carboximidamide

InChI

InChI=1S/C5H6N2S/c6-5(7)4-2-1-3-8-4/h1-3H,(H3,6,7)

InChIKey

QSELGEUCFNFITD-UHFFFAOYSA-N

Canonical SMILES

C1=CSC(=C1)C(=N)N

UNSPSC Code

12352100

Physical and chemical properties of Thiophene-2-carboximidamide

Boiling Point

220.8ºC at 760 mmHg

Density

1.36g/cm3

Exact Mass

126.02500

Flash Point

87.3ºC

H Bond Acceptors

2

H Bond Donors

2

Index of Refraction

1.675

LogP

1.83220

Molecular Formula

C5H6N2S

Molecular Weight

126.18000

PSA

78.11000

Safety Information of Thiophene-2-carboximidamide

Pictograms

Signal Word

Warning

Safety Data Sheet

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

Applications of Thiophene-2-carboximidamide

Thiophene-2-carboximidamide has several applications:

  • Pharmaceutical Development: Its derivatives are being explored for their potential as therapeutic agents due to their biological activities.
  • Chemical Research: Used as a building block in organic synthesis and material science.
  • Agricultural Chemistry: Investigated for potential use in agrochemicals due to its biological properties.

Interaction Studies of Thiophene-2-carboximidamide

Research on thiophene-2-carboximidamide has focused on its interactions with various biological targets. Notably, studies have demonstrated its ability to selectively inhibit nitric oxide synthase isoforms, which is significant for drug design aimed at treating diseases involving nitric oxide dysregulation. Additionally, interaction studies have explored its binding affinities and mechanisms of action at the molecular level.

Biological Activity of Thiophene-2-carboximidamide

Thiophene-2-carboximidamide has shown promising biological activities, particularly as an inhibitor of nitric oxide synthase. This inhibition can have implications in various therapeutic areas, including cardiovascular diseases and inflammation. Studies have indicated that derivatives of thiophene-2-carboximidamide exhibit selective inhibition of different isoforms of nitric oxide synthase, which is crucial for developing targeted therapies.

Retrosynthesis analysis of Thiophene-2-carboximidamide

  • Route#1

    Cas:54610-47-8
    Cas:54610-75-2
  • Route#2

    Cas:19402-64-3
    Cas:54610-60-5
    Cas:54610-75-2
  • Route#3

    Cas:54610-60-5
    Cas:54610-75-2