40398-30-9

Basic information

• Product Name: N-(morpholin-4-ylcarbothioyl)benzamide
• Synonyms: Benzamide, N-(4-morpholinylthioxomethyl)-; N-(Morpholin-4-ylcarbothioyl)benzamide; N1-morpholinocarbothioylbenzamide
• CAS NO: 40398-30-9
• Molecular Formula: C₁₂H₁₄N₂O₂S
• Molecular Weight: 250.3168
• Mol File: 40398-30-9.mol
• Article Data: 22

Chemical Properties

• Density: 1.277g/cm³
• Refractive Index: 1.618
• CAS DataBase Reference: N-(morpholin-4-ylcarbothioyl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(morpholin-4-ylcarbothioyl)benzamide(40398-30-9)
• EPA Substance Registry System: N-(morpholin-4-ylcarbothioyl)benzamide(40398-30-9)

Safety Data

• Hazardous Substances Data: 40398-30-9(Hazardous Substances Data)

Upstream product

• 110-91-8 morpholine 
• 98-88-4 benzoyl chloride 
• 333-20-0 potassium thioacyanate 
• 65-85-0 benzoic acid 
• 82655-60-5 N-(Morpholino-thiocarbonyl)benzimidchlorid 
• 540-72-7 sodium thiocyanide 
• 670-80-4 4-cyclohexen-1-ylmorpholine 
• 532-55-8 Benzoyl isothiocyanate 
• 936-52-7 1-(N-morpholino)cyclopent-1-ene 
• 1147550-11-5 ammonium thiocyanate 

Downstream Products

• 139933-22-5 4-Phenyl-5-(N-morpholinocarbonyl)-1,3,5-thiadiazol-2-thion 
• 76850-76-5 cis-bis(4-(benzoylthiocarbamoyl)morpholine)dichloroplatinum(II) 
• 76850-77-6 bis(N-(morpholinothiocarbonyl)benzamido)platinum(II) 
• 302328-85-4 cis-(S-dimethylsulfoxide)(N-morpholino-N'-(benzoyl)thioureato)chloroplatinum(II) 
• 76850-77-6 cis-bis(N-morpholino-N'-(benzoyl)thioureato)platinum(II) 
• 107111-48-8 4-(3-phenyl-1,2,4-oxadiazol-5-yl)morpholine 
• 22238-72-8 4-(5-phenyl-1,2,4-oxadiazol-3-yl)morpholine 
• 1338831-70-1 C₁₃H₁₆N₂O₂S 
• 55040-86-3 ethyl 2-(morpholin-4-yl)-4-phenylthiazole-5-carboxylate 
• 129880-85-9 2-(morpholin-4-yl)-4-phenylthiazole-5-carbaldehyde 

Relevant articles and documents

Heterocyclic lead(II) thioureato complexes as single-source precursors for the aerosol assisted chemical vapour deposition of PbS thin films

The lead N’-benzoylthioureato complexes of N-morpholine (1) and N-pyrrolidine (2) were synthesized and characterized by elemental analysis, Fourier Transform Infra-Red (FT-IR) spectroscopy, proton nuclear magnetic resonance (1H nmr) and thermogravimetric analyses (TGA). The X-ray single crystal structure of complex (1) was determined. The compounds were both used as single source precursors to deposit PbS films on glass substrates at 350, 400 and 450 °C using aerosol assisted chemical vapour deposition (AACVD) The surface morphology of PbS films were determined by scanning electron microscopy (SEM), the crystalline phases established by powder X-ray diffraction (p-XRD) analyses and composition by energy dispersive X-ray spectroscopy (EDX). The particle sizes were found to range between 82 and 85 nm from complex (1) and 70–105 nm for (2) The PbS films were studied by Near Infra-red (NIR) UV–Vis spectroscopy, band gap ranging from 1.46 to 1.55 eV were observed.

Synthesis and exploration of 2-morpholino-4-phenylthiazol-5-yl acrylamide derivatives for their effects against carbonic anhydrase I, II, IX and XII isoforms as a non-sulfonamide class of inhibitors

Novel series of 2-morpholino-4-phenylthiazol-5-yl acrylamide derivatives (8a–s) have been synthesized and explored as a non-sulfonamide class of carbonic anhydrase (CA, EC 4.2.1.1) inhibitors. The newly synthesized molecules were evaluated for their CA in

Pyrrole-thiazole based push-pull chromophores: An experimental and theoretical approach to structural, spectroscopic and NLO properties of the novel styryl dyes

Novel push-pull fluorophores constituted by two donors (substituted pyrrole and morpholine) linked to acceptor through thiazole electron spacer have been synthesized. The fluorophores are investigated for linear and non-linear optical properties by UV-VIS absorption and fluorescence spectroscopies, and by means of TD-DFT (B3LYP/6-31G(d)) method, with the aim of elucidating the ability of the morpholine/pyrrole-donor-thiazole-spacer based D-π-A fluorophores as organic NLO materials. The bond length alternation and generalized Mulliken-Hush (GMH) analysis is performed to understand the involvement of the donor in effective transfer of the charge to acceptor. Values of first-order hyperpolarizabilities (βCT or β0), obtained by the solvatochromic method (Lippert Mataga model), and the transition dipole moments (μeg) used to characterize and evaluate the non-linear optical performances of the D-π-A fluorophores in various microenvironments. The D-π-A fluorophores possess good values of βCT or β0 in different organic solvents and hold high thermal stabilities therefore can be used as potential organic NLO materials.