101078-51-7

Basic information

• Product Name: 6-Methoxy-2-(p-tolyl)benzo[d]thiazole
• Synonyms: Benzothiazole, 6-methoxy-2-(4-methylphenyl)-
• CAS NO: 101078-51-7
• Molecular Formula: C₁₅H₁₃NOS
• Molecular Weight: 255.33482
• Mol File: 101078-51-7.mol
• Article Data: 12

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 6-Methoxy-2-(p-tolyl)benzo[d]thiazole(CAS DataBase Reference)
• NIST Chemistry Reference: 6-Methoxy-2-(p-tolyl)benzo[d]thiazole(101078-51-7)
• EPA Substance Registry System: 6-Methoxy-2-(p-tolyl)benzo[d]thiazole(101078-51-7)

Safety Data

• Hazardous Substances Data: 101078-51-7(Hazardous Substances Data)

Upstream product

• 21011-45-0 4-methyl-N-(4-methoxyphenyl)benzothioamide 
• 104-87-0 4-methyl-benzaldehyde 
• 73011-26-4 6-methoxy-3H-benzo[d][1,2,3]dithiazole 2-oxide 
• 33667-91-3 N-(4-methoxyphenyl)-4-methylbenzamide 
• 874-60-2 4-methyl-benzoyl chloride 
• 99-94-5 p-Toluic acid 
• 2942-13-4 6-methoxy-1,3-benzothiazole 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 122-00-9 para-methylacetophenone 
• 6274-29-9 2-amino-5-methoxy-thiophenol 
• 214279-40-0 3-iodo-4-nitroanisol 
• 104-94-9 4-methoxy-aniline 

Downstream Products

• 101078-54-0 2-p-Tolyl-benzothiazol-6-ol 
• 101078-57-3 Acetic acid 2-p-tolyl-benzothiazol-6-yl ester 
• 101078-70-0 diethyl 4-(5-hydroxybenzo[d] thiazol-2-yl)benzylphosphonate 
• 101078-67-5 Acetic acid 2-[4-(diethoxy-phosphorylmethyl)-phenyl]-benzothiazol-6-yl ester 

Relevant articles and documents

A convenient access to substituted benzothiazole scaffolds via intramolecular cyclization of thioformanilides

A new and practical method has been developed for the synthesis of substituted benzothiazoles via the intramolecular cyclization of thioformanilides using DDQ in CH2Cl2 at ambient temperature. The reaction proceeds in high yields via

Hypervalent iodine mediated intramolecular cyclization of thioformanilides: Expeditious approach to 2-substituted benzothiazoles

A new, mild, and efficient method has been developed for the synthesis of 2-substituted benzothiazoles via the intramolecular cyclization of thioformanilides by using hypervalent iodine reagents in CH2Cl 2 at ambient temperature. The

Metal-Free Synthesis of 2-Arylbenzothiazoles from Aldehydes, Amines, and Thiocyanate

A highly efficient method for the synthesis of 2-arylbenzothiazoles has been developed using readily available aromatic amines, benzaldehydes, and NH4SCN as a sulfur source. A library of 2-arylbenzothiazoles with wide functional group compatibility has been synthesized in good yields through iodine-mediated oxidative annulation.

Synthesis of 2-substituted benzothiazoles from 1-iodo-2-nitrobenzenes by a copper-catalyzed one-pot three-component reaction

A novel method was developed for synthesizing 2-substituted 1,3-benzothiazoles through a copper-catalyzed, one-pot, three-component reaction of a 1-iodo-2-nitrobenzene with sodium sulfide and an aldehyde. Georg Thieme Verlag Stuttgart - New York.