600179-91-7

Basic information

• Product Name: 1,3-Azulenedicarboxylic acid, 6-(3,6-dihydro-4,5-dimethyl-1-oxido-2H-1,2-thiazin-2-yl)-, diethyl ester
• CAS NO: 600179-91-7
• Molecular Formula: C22H25NO5S
• Mol File: 600179-91-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1,3-Azulenedicarboxylic acid, 6-(3,6-dihydro-4,5-dimethyl-1-oxido-2H-1,2-thiazin-2-yl)-, diethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Azulenedicarboxylic acid, 6-(3,6-dihydro-4,5-dimethyl-1-oxido-2H-1,2-thiazin-2-yl)-, diethyl ester(600179-91-7)
• EPA Substance Registry System: 1,3-Azulenedicarboxylic acid, 6-(3,6-dihydro-4,5-dimethyl-1-oxido-2H-1,2-thiazin-2-yl)-, diethyl ester(600179-91-7)

Safety Data

• Hazardous Substances Data: 600179-91-7(Hazardous Substances Data)

Upstream product

• 513-81-5 2,3-dimethyl-buta-1,3-diene 
• 600179-88-2 N-sulfinyl-1,3-bis(ethoxycarbonyl)-6-azulenylamine 

Relevant articles and documents

Preparation, characterization, and cycloaddition reaction of the heterocumulenes attached directly to azulenes. An efficient strategy for the preparation of azulene-substituted heterocycles

Preparation and cycloaddition reaction of novel azulene-substituted N-sulfinylamines 1 and 2 are reported. The influence of the -N=S=O group on the UV-vis and NMR spectra of the azulene ring to which it is bonded is discussed. X-ray crystal analysis of 1 revealed the syn-configuration and the twisted structure of the N-sulfinylamine moiety. The synthetic utility of 1 and 2 have been explored by the cycloaddition reaction to afford novel azulene-substituted heterocycles under high-pressure conditions. We also described herein the synthesis and some properties of related 2-azulenylisothiocyanate.