423738-98-1

Basic information

• Product Name: 4-(6-nitrobenzo[d]thiazol-2-yl)Morpholine
• Synonyms: 4-(6-nitrobenzo[d]thiazol-2-yl)Morpholine;2-(morpholin-4-yl)-6-nitro-1,3-benzothiazole
• CAS NO: 423738-98-1
• Molecular Formula: C₁₁H₁₁N₃O₃S
• Molecular Weight: 265.28834
• Mol File: 423738-98-1.mol
• Article Data: 11

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-(6-nitrobenzo[d]thiazol-2-yl)Morpholine(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(6-nitrobenzo[d]thiazol-2-yl)Morpholine(423738-98-1)
• EPA Substance Registry System: 4-(6-nitrobenzo[d]thiazol-2-yl)Morpholine(423738-98-1)

Safety Data

• Hazardous Substances Data: 423738-98-1(Hazardous Substances Data)

Upstream product

• 110-91-8 morpholine 
• 4845-58-3 2-mercapto-6-nitrobenzothiazole 
• 2407-11-6 2-chloro-6-nitrobenzothiazole 
• 2131-61-5 p-nitrophenyl isothiocyanate 
• 6285-57-0 2-amino-6-nitrobenzothiazole 
• 364339-83-3 N-(4-nitrophenyl)-N’-morpholinothiourea 
• 4845-58-3 6-nitrobenzo[d]thiazole-2(3H)-thione 
• 149-30-4 2-thioxo-3H-1,3-benzothiazole 
• 137-07-5 2-amino-benzenethiol 

Downstream Products

• 1400420-80-5 4-(6-(4-phenyl-1H-1,2,3-triazol-1-yl)benzo[d]thiazol-2-yl)morpholine 
• 850021-27-1 2-morpholinobenzo[d]thiazol-6-amine 

Relevant articles and documents

A Mild Synthesis of 2-Substituted Benzothiazoles via Nickel-Catalyzed Intramolecular Oxidative C-H Functionalization

A highly efficient synthetic method for the preparation of 2-aminobenzothiazoles starting from arylthioureas has been reported. By using a nickel catalyst, arylthioureas undergo intramolecular oxidative C-H bond functionalization, giving the desired 2-aminobenzothiazoles in good to excellent yields. This protocol features an inexpensive catalyst, low catalyst loading, mild reaction conditions, a short reaction time, and good to excellent yields, and it can be scaled up easily to a gram scale with almost no yields decreasing.

Eosin y catalyzed visible-light-promoted aerobic oxidative cyclization of 2-aminobenzothiazole

A mild and efficient one-pot visible light irradiated synthesis of 2-aminobenzothiazole 4(a-l) from arylisothiocyanate 1(a-l) and secondary amines 2 have been reported in presence of eosin Y as an organophotoredox catalyst at room temperature under aerobi

Arylation of amines and monoarylation of symmetrical diamines in the presence of brine solution with diheteroaryl halides

A simple, scalable, ligand-free, and metal-free protocol for arylation of amines and monoarylation of symmetrical diamines with diheteroaryl halides in the presence of brine solution has been developed. The protocol has broad structural applicability for chemoselective monoarylation of a wide variety of symmetrical, cyclic, and acyclic aliphatic diamines. The protocol is also applicable for selective arylation of aliphatic amine in the presence of aromatic amine.