1392102-38-3

Basic information

• Product Name: (S)-3,10-dibromo-6-phenyl-6H-benzo[5,6][1,3]oxazino[3,4-a]indole
• Synonyms: (S)-3,10-dibromo-6-phenyl-6H-benzo[5,6][1,3]oxazino[3,4-a]indole;(6S)-3,10-Dibromo-6-phenyl-6H-indolo[1,2-c][1,3]benzoxazine;6H-Indolo[1,2-c][1,3]benzoxazine, 3,10-dibromo-6-phenyl-, (6S)-;Elbasvir N-1
• CAS NO: 1392102-38-3
• Molecular Formula: C₂₁H₁₃Br₂NO
• Molecular Weight: 455.14202
• EINECS: 1592732-453-0
• Mol File: 1392102-38-3.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 606.8±55.0 °C(Predicted)
• Appearance: /
• Density: 1.68±0.1 g/cm3(Predicted)
• CAS DataBase Reference: (S)-3,10-dibromo-6-phenyl-6H-benzo[5,6][1,3]oxazino[3,4-a]indole(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-3,10-dibromo-6-phenyl-6H-benzo[5,6][1,3]oxazino[3,4-a]indole(1392102-38-3)
• EPA Substance Registry System: (S)-3,10-dibromo-6-phenyl-6H-benzo[5,6][1,3]oxazino[3,4-a]indole(1392102-38-3)

Safety Data

• Hazardous Substances Data: 1392102-38-3(Hazardous Substances Data)

Usage

General Description

(S)-3,10-dibromo-6-phenyl-6H-benzo[5,6][1,3]oxazino[3,4-a]indole is a chemical compound with a complex and unique structure. It is a dibromo derivative of benzo[5,6][1,3]oxazino[3,4-a]indole, which is a bicyclic heterocycle. The compound contains bromine atoms at the 3 and 10 positions and a phenyl group at the 6 position. (S)-3,10-dibromo-6-phenyl-6H-benzo[5,6][1,3]oxazino[3,4-a]indole has potential applications in medicinal chemistry and drug discovery due to its unique structure and potential pharmacological properties. It may also be of interest in the field of organic synthesis and chemical research, where its complex structure and reactivity could be explored for the development of new synthetic methodologies.

Upstream product

• 589-21-9 (4-bromophenyl)hydrazine 
• 618-31-5 benzylidene dibromide 
• 1246471-94-2 5-bromo-2-(5-bromo-1H-indol-2-yl)phenol 
• 1585969-16-9 (6S,12aR)-3,10-dibromo-6-phenyl-12,12a-dihydro-6H-benzo-[5,6][1,3]oxazino[3,4-a]indole 
• 1585969-24-9 (R)-2-(1-amino-2-(2,5-dibromophenyl)ethyl)-5-bromophenol 
• 1585969-22-7 5-bromo-2-(2-(2,5-dibromophenyl)-1-iminoethyl)phenol 
• 1403991-85-4 1-(4-bromo-2-hydroxyphenyl)-2-(2,5-dibromophenyl)ethanone 
• 1585969-17-0 (R)-5-bromo-2-(5-bromoindolin-2-yl)phenol 
• 1403991-82-1 3-bromophenyl 2-(2,5-dibromophenyl)acetate 
• 100-52-7 benzaldehyde 
• 1369594-56-8 3,10-dibromo-6-phenyl-6H-benzo[5,6][1,3]oxazino[3,4-a]indole 
• 1369594-43-3 C₁₄H₁₂Br₂N₂O 
• 30186-18-6 4'-bromo-2'-hydroxyacetophenone 
• 75-91-2 tert.-butylhydroperoxide 

Downstream Products

• 1585969-26-1 (2S,2'S)-di-tert-butyl 2,2'-(5,5'-((S)-6-phenyl-6H-benzo[5,6][1,3]oxazino[3,4-a]indole-3,10-diyl)bis(1H-imidazole-5,2-diyl))bis(pyrrolidine-1-carboxylate) 4-nitrobenzoic acid 
• 1585969-27-2 6-phenyl-3,10-bis(2-((S)-pyrrolidin-2-yl)-1H-imidazol-5-yl)-6H-benzo[5,6][1,3]oxazino[3,4-a]indole 
• 1370468-36-2 N,N'-[[(6S)-6-phenyl-6H-indolo[1,2-c][1,3]benzoxazine-3,10-diyl]bis[1H-imidazole-5,2-diyl-(2S)-2,1-pyrrolidinediyl-[(1S)-1-(1-methylethyl)-2-oxo-2,1-ethanediyl]]]bis[carbamic acid] C,C'-dimethyl ester 

Relevant articles and documents

Facile Quantum Yield Determination via NMR Actinometry

A simplified approach to quantum yield (φ) measurement using in situ LED NMR spectroscopy has been developed. The utility and performance of NMR actinometry has been demonstrated for the well-known chemical actinometers potassium ferrioxalate and o-nitrobenzaldehyde. A novel NMR-friendly actinometer, 2,4-dinitrobenzaldehyde, has been introduced for both 365 and 440 nm wavelengths. The method has been utilized successfully to measure the quantum yield of several recently published photochemical reactions.

Multi-substituted BODIPY organic photocatalyst catalytic indole oxazolines oxidative dehydrogenation synthesis of indole compounds method

The invention discloses a method for catalyzing synthesis of an indole compound by oxidative dehydrogenation of an indoline compound through a polysubstituted BODIPY organic photocatalyst. The method is characterized in that air or oxygen is taken as an oxidizing agent instead of peroxide, and a polysubstituted BODIPY organic compound serving as a non-metal photocatalyst is used in a reaction. The method has the advantages of small using amount of the catalyst, high catalytic efficiency, mild reaction conditions, easiness in operation environmental friendliness, high product conversion rate and high selectivity, and can be applied to synthesis of nuclear molecules of medicine elbasvir for treating hepatitis C viruses.

Matched and mixed cap derivatives in the tetracyclic indole class of HCV NS5A inhibitors

A matched and mixed capping SAR study was conducted on the tetracyclic indole class of HCV NS5A inhibitors to examine the influence of modifications of this region on the overall HCV virologic resistance profiles.