76148-93-1

Basic information

• Product Name: 3-(4-METHOXY-PHENYL)-2H-BENZO[1,4]THIAZINE
• Synonyms: 3-(4-METHOXY-PHENYL)-2H-BENZO[1,4]THIAZINE;3-(4-methoxyphenyl)-2H-1,4-benzothiazine
• CAS NO: 76148-93-1
• Molecular Formula: C₁₅H₁₃NOS
• Molecular Weight: 255.33
• Mol File: 76148-93-1.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 389.6°C at 760 mmHg
• Flash Point: 189.4°C
• Appearance: /
• Density: 1.19g/cm³
• Vapor Pressure: 6.3E-06mmHg at 25°C
• Refractive Index: 1.631
• CAS DataBase Reference: 3-(4-METHOXY-PHENYL)-2H-BENZO[1,4]THIAZINE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-METHOXY-PHENYL)-2H-BENZO[1,4]THIAZINE(76148-93-1)
• EPA Substance Registry System: 3-(4-METHOXY-PHENYL)-2H-BENZO[1,4]THIAZINE(76148-93-1)

Safety Data

• Hazardous Substances Data: 76148-93-1(Hazardous Substances Data)

Usage

InChI:InChI=1/C15H13NOS/c1-17-12-8-6-11(7-9-12)14-10-18-15-5-3-2-4-13(15)16-14/h2-9H,10H2,1H3

Upstream product

• 2632-13-5 2-Bromo-4'-methoxyacetophenone 
• 52380-58-2 sodium 2-aminothiophenol 
• 137-07-5 2-amino-benzenethiol 

Downstream Products

• 76148-60-2 3-(4-methoxyphenyl)-2H-benzo[b][1,4]thiazin-2-one 
• 1041166-99-7 3-(4-methoxyphenyl)-3,4-dihydro-2H-benzo[b][1,4]thiazine 
• 1429933-83-4 (S)-3-(4-methoxyphenyl)-3,4-dihydro-2H-benzo[b]-[1,4]thiazin-2-one 
• 76148-59-9 Δ^2,2'-bi-<(3-p-methoxyphenyl)-2H-1,4-benzothiazine> 
• 6265-92-5 2-(4-methoxy-phenyl)-benzothiazole 
• 76148-56-6 3,3'-bis(4-methoxyphenyl)-2H,2'H-2,2'-bibenzo[b][1,4]thiazine 
• 76148-95-3 2-(p-methoxycarbonylphenylhydrazono)-3-(p-methoxyphenyl)-2H-1,4-benzothiazine 
• 76148-69-1 3-(p-methoxyphenyl)-2-(p-nitrobenzylhydrazono)-2H-1,4-benzothiazine 

Relevant articles and documents

Bioglycerol-based sulfonic acid-functionalized carbon catalyst as an efficient and reusable catalyst for one-pot synthesis of 3- substituted-2 h -1,4-benzothiazines

A simple and efficient synthetic protocol has been developed for the synthesis of 3-substituted-2H-1,4-benzothiazines by using bioglycerol-based sulfonic acid-functionalized carbon catalyst, devoid of corrosive acidic and basic reagents. The developed met

From phenothiazine to 3-phenyl-1,4-benzothiazine derivatives as inhibitors of the Staphylococcus aureus NorA multidrug efflux pump

Overexpression of efflux pumps is an important mechanism by which bacteria evade effects of substrate antimicrobial agents and inhibition of such pumps is a promising strategy to circumvent this resistance mechanism. NorA is a Staphylococcus aureus multid