5667-03-8

Basic information

• Product Name: 2-Phenyl-1,5-benzothiazepin-4(5H)-one
• Synonyms: 2-Phenyl-1,5-benzothiazepin-4(5H)-one
• CAS NO: 5667-03-8
• Molecular Formula: C₁₅H₁₁NOS
• Molecular Weight: 253.3189
• Mol File: 5667-03-8.mol

Chemical Properties

• Boiling Point: 458.3°Cat760mmHg
• Flash Point: 231°C
• Appearance: /
• Density: 1.257g/cm³
• Vapor Pressure: 1.39E-08mmHg at 25°C
• Refractive Index: 1.656
• CAS DataBase Reference: 2-Phenyl-1,5-benzothiazepin-4(5H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Phenyl-1,5-benzothiazepin-4(5H)-one(5667-03-8)
• EPA Substance Registry System: 2-Phenyl-1,5-benzothiazepin-4(5H)-one(5667-03-8)

Safety Data

• Hazardous Substances Data: 5667-03-8(Hazardous Substances Data)

Usage

InChI:InChI=1/C15H11NOS/c17-15-10-14(11-6-2-1-3-7-11)18-13-9-5-4-8-12(13)16-15/h1-10H,(H,16,17)

Upstream product

• 136-95-8 2-amino-benzthiazole 
• 27068-82-2 3-hydroxy-2-phenyl-2,3-dihydro-5H-benzo[b][1,4]thiazepin-4-one 
• 137-07-5 2-amino-benzenethiol 
• 637-44-5 phenylpropyolic acid 
• 31966-80-0 3-acetoxy-2-phenyl-2,3-dihydro-5H-benzo[b][1,4]thiazepin-4-one 

Downstream Products

• 120-75-2 2-Methylbenzothiazole 
• 2584-37-4 1-methyl-4-phenyl-1H-quinolin-2-one 
• 97038-01-2 5-methyl-2-phenyl-2,3-dihydrobenzo[b][1,4]thiazepin-4(5H)-one 
• 104505-72-8 2-benzylidene <1,4>benzothiazine-3-one 
• 98-86-2 acetophenone 
• 104505-69-3 4-Methoxy-2-phenyl-1,5-benzothiazepin 
• 29476-22-0 (R)-2-phenyl-2,3-dihydrobenzo[b][1,4]thiazepin-4(5H)-one 
• 5845-26-1 5-(2-(dimethylamino)ethyl)-2-phenyl-2,3-dihydrobenzo[b][1,4]thiazepin-4(5H)-one 
• 1428258-32-5 5-(4-methoxybenzyl)-2-phenyl-2,3-dihydrobenzo[b][1,4]thiazepin-4(5H)-one 

Relevant articles and documents

Rh-Catalyzed Asymmetric Hydrogenation of Unsaturated Medium-Ring NH Lactams: Highly Enantioselective Synthesis of N-Unprotected 2,3-Dihydro-1,5-benzothiazepinones

A straightforward method to prepare 1,5-benzothiazepines was reported. Catalyzed by a Rh/Zhaophos complex, unsaturated cyclic NH lactams with a medium-size ring were hydrogenated smoothly, giving remarkably high enantioselectivities. The sulfur atom in the substrates did not bring an inhibition which was observed with commercially available bisphosphine ligands. This method was successfully applied in the scale-up synthesis of (R)-(-)-thiazesim.

Asymmetric Hydrogenation of Vinylthioethers: Access to Optically Active 1,5-Benzothiazepine Derivatives

A novel asymmetric hydrogenation of vinylthioethers was developed using a ruthenium(II) NHC complex. This method provides an efficient approach to optically active 1,5-benzothiazepines featuring stereocenters with C-S bonds. Excellent enantioselectivities

Unexpected Reaction Pathways in the Reaction of Alkoxyalkynyl-chromium(0) Carbenes with Aromatic Dinucleophiles

Thermal- or SiO2-induced reactions of the Michael adducts of 1,2-aromatic dinucleophiles and alkynyl-chromium(0) carbene complexes, compounds 7-10, form different products in good yields depending on the nature of the aromatic dinucleophile used. Thus, 1,2-diaminobenzene derivatives 7 and 8 rearrange to pentacarbonylchromium(0) isocyanide complexes 11, 12, 14, and 15 in a process that occurs through bicyclic intermediates 24. Adducts 9 derived from o-aminophenol give 2,3-dihydro-1,5-benzoxazepine derivatives 17 by intramolecular 1,2-addition, followed by protonation at the chromium center and reductive elimination. In contrast, base-promoted addition of the phenolic hydroxy group in compound 9a affords 3-ethoxy-5-phenyl-5,6-dihydro-2H-1,6-benzoxazocin-2-one (18), together with the expected adduct 17a. Compound 18 is formed by a nucleophilic addition to a CO ligand in a preformed carbene complex. This is a new example of the rare attack of a nucleophile on a CO ligand in a Fischer carbene complex. Adducts 10 form seven-membered-ring carbene complexes 19 and 20 by intramolecular aminolysis. In contrast, reaction of alkynyl carbene complexes with 1,8-diaminonaphthalene under very mild conditions leads to 2-substituted perimidines 33 together with the corresponding ethoxymethylmetal carbene complex 32 through an unprecedented fragmentation process in a formal retro-Aumann reaction.

Studies of annelated 1,4-benzothiazines and 1,5-benzothiazepines. VII. Synthesis and inhibition of benzodiazepine receptor binding of some 4,5-dihydro-tetrazolo[5,1-d]-1,5-benzothiazepines and 5-phenyl-s-triazolo[3,4-d]-1,5-benzothiazepines

The 4,5-dihydro-tetrazolo[5,1-d]-1,5-benzothiazepines 3a-k and the 5-phenyl-s-triazolo[3,4-d]-1,5-benzothiazepines 6a-f and 11a-c have been prepared and tested for their ability to displace [H] flunitrazepam binding from bovine brain membranes. Some of th

Note on the Synthesis, Properties, and Reactions of 4-Methoxy-2-phenyl-1,5-benzothiazepine

The title compound 3 is synthesized by O-alkylation of the corresponding lactam 1.The behaviour of 3 is different from a compound with the same formula which has been published recently in this journal; the structure of 3 therefore was confirmed by X-ray

Rearrangements and Complex Eliminations with 1,5-Benzothiazepin-4-ones

The 1,5-benzothiazepin-4-ones 3, 5, and 7 - 10 are pyrolyzed (with proton catalysis in part).New or rarely documented rearrangements and complex eliminations occur.These are classified and mechanistically discussed.The products and by-products are spectroscopically characterized (IR, UV, NMR, MS).Their configurations are elucidated via photolysis experiments. 4 photodimerizes in solution and in the crystalline state with great ease to give 14. 11 is remarkably insensitive towards hydrolysis.