136507-00-1

Basic information

• Product Name: 3-(2-benzthiazolyl)-6-propyl-7-O-(N-tert-butyloxycarbonyl-6-aminocaproyl)chromone
• Synonyms: 3-(2-benzthiazolyl)-6-propyl-7-O-(N-tert-butyloxycarbonyl-6-aminocaproyl)chromone
• CAS NO: 136507-00-1
• Molecular Weight: 550.676
• Mol File: 136507-00-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-(2-benzthiazolyl)-6-propyl-7-O-(N-tert-butyloxycarbonyl-6-aminocaproyl)chromone(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(2-benzthiazolyl)-6-propyl-7-O-(N-tert-butyloxycarbonyl-6-aminocaproyl)chromone(136507-00-1)
• EPA Substance Registry System: 3-(2-benzthiazolyl)-6-propyl-7-O-(N-tert-butyloxycarbonyl-6-aminocaproyl)chromone(136507-00-1)

Safety Data

• Hazardous Substances Data: 136507-00-1(Hazardous Substances Data)

Upstream product

• 6404-29-1 6-(tert-butoxycarbonylamino)hexanoic acid 
• 136506-95-1 3-Benzothiazol-2-yl-7-hydroxy-6-propyl-chromen-4-one 

Relevant articles and documents

CHEMISTRY OF HETEROANALOGS OF ISOFLAVONES. 16. BENZTHIAZOLE ANALOGS OF ISOFLAVONES

The reaction of α-(2-benzthiazolyl)-2,4-dihydroxy-5-alkylacetophenones with anhydrides and chlorides of carboxylic acids yielded 3-(2-benzthiazolyl)chromones with electron-acceptor and electron donor substituents, as well as chromones unsubstituted in the 2-position.Their acylation, alkylation, and aminoacylation reactions and their interaction with electrophilic and nucleophilic reagents were studied.