896469-22-0

Basic information

• Product Name: (1-(2-fluorophenyl)-N-(4-methylbenzo[d]thiazol-2-yl)methanimine)
• Synonyms: (1-(2-fluorophenyl)-N-(4-methylbenzo[d]thiazol-2-yl)methanimine)
• CAS NO: 896469-22-0
• Molecular Weight: 270.33
• Mol File: 896469-22-0.mol

Chemical Properties

• CAS DataBase Reference: (1-(2-fluorophenyl)-N-(4-methylbenzo[d]thiazol-2-yl)methanimine)(CAS DataBase Reference)
• NIST Chemistry Reference: (1-(2-fluorophenyl)-N-(4-methylbenzo[d]thiazol-2-yl)methanimine)(896469-22-0)
• EPA Substance Registry System: (1-(2-fluorophenyl)-N-(4-methylbenzo[d]thiazol-2-yl)methanimine)(896469-22-0)

Safety Data

• Hazardous Substances Data: 896469-22-0(Hazardous Substances Data)

Upstream product

• 1477-42-5 4-methyl-1,3-benzothiazol-2-amine 
• 446-52-6 2-Fluorobenzaldehyde 

Downstream Products

• 1245712-05-3 dimethyl 2-((4-methylbenzo[d]thiazol-2-ylamino)(2-fluorophenyl)methyl)malonate 
• 1245711-67-4 diethyl 2-((4-methylbenzo[d]thiazol-2-ylamino)(2-fluorophenyl)-methyl)malonate 
• 1367487-37-3 diethyl 2-((4-methylbenzo[d]thiazol-2-ylamino)(2-fluorophenyl)-methyl)malonate 
• 1135520-87-4 diethyl ((2-fluorophenyl)((4-methylbenzo[d]thiazol-2-yl)amino)methyl)phosphonate 
• 882182-49-2 ((2-fluorophenyl)(4-methylbenzothiazol-2-ylamino)methyl)phosphonic acid diethyl ester 
• 1135520-85-2 (R)-dufulin 

Relevant articles and documents

Chiral cinchona alkaloid-thiourea catalyzed mannich reaction for enantioselective synthesis of β-amino ketones bearing benzothiazol moiety

Mannich reactions of imine with acetylacetone were effectively catalyzed by the modified chiral cinchona alkaloid-derived thiourea. The reactions led to chiral β-amino carbonyl compounds in high yields and good enantioselectivities. The study demonstrated

A compound with anti-virus activity of the benzothiazole heterocyclic chiral α - aminophosphonic acid ester compound and its preparation and use

The present invention discloses a class of chiral alpha-amino phosphonate ester compounds having anti-virus activity and containing benzothiazole heterocycle, preparation and applications thereof, wherein the structure of the compound is represented by th

Asymmetric synthesis and bioselective activities of α-amino-phosphonates based on the dufulin motif

The asymmetric synthesis of enantiomerically pure α-aminophosphonates with high and bioselective activities is a challenge. Here, we report that both enantiomers of α-aminophosphonates bearing the N-benzothiazole moiety can be prepared in high yields (up

Enantioselective synthesis of β-amino esters bearing a benzothiazole moiety via a Mannich-type reaction catalyzed by a cinchona alkaloid derivative

Novel β-amino esters bearing a bioactive benzothiazole moiety were obtained with high enantioselectivities (up to 95 % ee) through a Mannich-type reaction of different imines with malonate in the presence of a new chiral cinchona alkaloid thiourea catalys