104505-74-0

Basic information

• Product Name: 2-benzyl-3-oxo-3,4-dihydro-2H-1,4-benzothiazine
• Synonyms: 2-benzyl-3-oxo-3,4-dihydro-2H-1,4-benzothiazine
• CAS NO: 104505-74-0
• Molecular Weight: 255.34
• Mol File: 104505-74-0.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2-benzyl-3-oxo-3,4-dihydro-2H-1,4-benzothiazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-benzyl-3-oxo-3,4-dihydro-2H-1,4-benzothiazine(104505-74-0)
• EPA Substance Registry System: 2-benzyl-3-oxo-3,4-dihydro-2H-1,4-benzothiazine(104505-74-0)

Safety Data

• Hazardous Substances Data: 104505-74-0(Hazardous Substances Data)

Upstream product

• 62-53-3 aniline 
• 101308-40-1 ethyl 2-bromo-3-phenylpropionate 
• 137-07-5 2-amino-benzenethiol 
• 118670-85-2 (2E)-N-(2-iodophenyl)-3-phenylprop-2-enamide 
• 55043-20-4 2-(phenylmethylidene)-3,4-dihydro-2H-1,4-benzothiazin-3-one 
• 935524-52-0 2-(2-amino-phenylsulfanyl)-3-phenyl-propionic acid methyl ester 
• 70288-60-7 methyl 2-bromo-3-phenylpropionate 
• 29476-22-0 2,3-dihydro-2-phenyl-1,5-benzothiazepin-4(5H)-one 
• 93102-82-0 2-acetyl-3-oxo-3,4-dihydro-2H-1,4-benzothiazine 
• 100-39-0 benzyl bromide 
• 16503-53-0 2-bromo-3-phenylpropanoic acid 
• 103-36-6 ethyl 3-phenyl-2-propenoate 
• 97195-31-8 cinnamic acid-(2-mercapto-anilide) 

Downstream Products

• 935524-53-1 2-Benzyl-3,4-dihydro-2H-1,4-benzothiazine 

Relevant articles and documents

Synthesis of Oxazine, Thiazine, and Quinoxaline Derivatives Containing a Benzyl Fragment from 3-Aryl-2-Bromopropanoic Acids and Their Esters

Abstract: 3-Aryl-2-bromopropanoic acid esters reacted with o-phenylenediamine, 2-sulfanylaniline, and L-cysteine to give quinoxaline, 1,4-thiazine, and thiomorpholine derivatives, respectively, containing an aryl-methyl substituent. Analogous 1,4-benzoxaz

LXR modulators

A compound of formula I wherein A, X, q, R1, R2a, R2b, R2c, R3a, and R3b are defined herein.

Studies on antidiabetic agents. IX. A new aldose reductase inhibitor, AD-5467, and related 1,4-benzoxazine and 1,4-benzothiazine derivatives: Synthesis and biological activity

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