7210-75-5

Basic information

• Product Name: 2-BENZOYLTHIAZOLE
• Synonyms: 2-BENZOYLTHIAZOLE;Phenyl(2-thiazolyl) ketone
• CAS NO: 7210-75-5
• Molecular Formula: C₁₀H₇NOS
• Molecular Weight: 189.23
• Mol File: 7210-75-5.mol
• Article Data: 14

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-BENZOYLTHIAZOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-BENZOYLTHIAZOLE(7210-75-5)
• EPA Substance Registry System: 2-BENZOYLTHIAZOLE(7210-75-5)

Safety Data

• Hazardous Substances Data: 7210-75-5(Hazardous Substances Data)

Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 74, p. 6260, 1952 DOI: 10.1021/ja01144a031

Upstream product

• 65-85-0 benzoic acid 
• 288-47-1 1,3-thiazole 
• 10364-94-0 1-benzoylimidazole 
• 98-88-4 benzoyl chloride 
• 140-29-4 phenylacetonitrile 
• 18732-64-4 2-benzyl-4,5-dihydro-thiazole 
• 3034-53-5 2-bromo-1,3-thiazole 
• 100-47-0 benzonitrile 
• 100-52-7 benzaldehyde 
• 134271-25-3 [1-Phenyl-1-thiazol-2-yl-meth-(E)-ylidene]-hydrazine 
• 134271-25-3 [1-Phenyl-1-thiazol-2-yl-meth-(Z)-ylidene]-hydrazine 
• 40610-14-8 2-lithiothiazole 
• 79265-30-8 2-(trimethylsilyl)thiazole 
• 134271-27-5 3-Phenyl-1,2,3-triazolo<5,1-b>thiazole 

Downstream Products

• 132499-96-8 BTNPHTS 
• 133543-90-5 3-(2-thiazolylcarbonyl)benzenesulfonic acid 
• 134271-25-3 [1-Phenyl-1-thiazol-2-yl-meth-(Z)-ylidene]-hydrazine 
• 134271-25-3 [1-Phenyl-1-thiazol-2-yl-meth-(E)-ylidene]-hydrazine 
• 1086277-38-4 (E/Z)-ethyl 3-phenyl-3-(thiazol-2-yl)prop-2-enoate 
• 1452128-83-4 2-(1-phenylvinyl)thiazole 
• 24295-16-7 7-oxy-8-phenyl-thiazolo[3,2-a]pyrazinylium; bromide 
• 24288-01-5 8-phenyl-thiazolo[3,2-a]pyrazinylium; bromide 
• 93001-83-3 2-(α-Phenylacetoxymethyl)thiazole 
• 134271-31-1 2-(Dibromo-phenyl-methyl)-thiazole 
• 879-52-7 phenyl-thiazol-2-yl-methanol 
• 134271-27-5 3-Phenyl-1,2,3-triazolo<5,1-b>thiazole 
• 24295-07-6 phenyl-thiazol-2-yl-methanone oxime 

Relevant articles and documents

Photoinduced remote heteroaryl migration accompanied by cyanoalkylacylation in continuous flow

A photoinduced 1,4-heteroaryl migration from a carbon center to a nitrogen center accompanied by a cyanoalkylacylation of heterocyclic-substituted azidyl homoallylic alcohols and cycloketone oxime esters has been described. This simple and powerful protoc

A convenient synthesis of 2-acyl benzothiazoles/thiazoles from benzothiazole/thiazole and N,N'-carbonyldiimidazole activated carboxylic acids

A convenient and efficient strategy for the synthesis of 2-acyl benzothiazoles/thiazoles has been developed. The treatment of benzothiazole/thiazole with allylic Grignard reagents readily generates the corresponding 2-Grignard reagents, which is followed by a reaction with N,N'-carbonyldiimidazole activated carboxylic acids to afford various 2-acyl benzothiazoles/thiazoles products. The synthetic method is applicable to a wide array of carboxylic acids and allows easy access to 2-acyl benzothiazoles/thiazoles with considerable yields under mild reaction conditions.

DDQ-induced dehydrogenation of heterocycles for c-c double bond formation: Synthesis of 2-thiazoles and 2-oxazoles

Strong as an Ox: 2-Thiazoles and 2-oxazoles are formed by oxidation of 2-thiazolines and 2-oxazolines without requiring substituents at the C4 and C5 positions. DDQ plays an important role as the oxidant in this transformation and metal is unnecessary. This general procedure shows good functional group tolerance and provides a wide variety of 2-thiazoles and 2-oxazoles in moderate to excellent yields.