1262518-46-6

Basic information

• Product Name: 3-(4-piperidin-4-ylidene-4H-1-thiabenzo[f]azulen-2-yl)-propionic acid benzenesulfonate
• Synonyms: 3-(4-piperidin-4-ylidene-4H-1-thiabenzo[f]azulen-2-yl)-propionic acid benzenesulfonate
• CAS NO: 1262518-46-6
• Molecular Weight: 509.647
• Mol File: 1262518-46-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-(4-piperidin-4-ylidene-4H-1-thiabenzo[f]azulen-2-yl)-propionic acid benzenesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-piperidin-4-ylidene-4H-1-thiabenzo[f]azulen-2-yl)-propionic acid benzenesulfonate(1262518-46-6)
• EPA Substance Registry System: 3-(4-piperidin-4-ylidene-4H-1-thiabenzo[f]azulen-2-yl)-propionic acid benzenesulfonate(1262518-46-6)

Safety Data

• Hazardous Substances Data: 1262518-46-6(Hazardous Substances Data)

Upstream product

• 1262518-42-2 3-[4-(1-tert-butoxycarbonylpiperidin-4-ylidene)-9,10-dihydro-4H-1-thiabenzo[f]azulen-2-yl]acrylic acid 
• 1262518-41-1 3-[4-(1-ethoxycarbonylpiperidin-4-ylidene)-9,10-dihydro-4H-1-thiabenzo[f]azulen-2-yl]acrylic acid 
• 1262518-43-3 3-[4-(1-tert-butoxycarbonylpiperidin-4-ylidene)-4H-1-thiabenzo[f]azulen-2-yl]propionic acid 
• 23455-54-1 4-(9,10-dihydro-benzo[4,5]cyclohepta[1,2-b]thiophen-4-ylidene)-piperidine-1-carboxylic acid ethyl ester 
• 1176739-94-8 ethyl 3-[4-(1-tert-butoxy-carbonylpiperidin-4-ylidene)-4H-1-thiabenzo[f]azulen-2-yl]-propionate 
• 1176739-93-7 ethyl 4-[2-(2-ethoxycarbonylvinyl)-9,10-dihydro-1-thiabenzo[f]azulen-4-ylidene]piperidine-1-carboxylate 
• 1176738-35-4 3-(4-piperidin-4-ylidene-9,10-dihydro-4H-1-thiabenzo[f]azulen-2-yl)acrylic acid 
• 1176739-91-5 Ethyl 4-(2-bromo-9,10-dihydro-1-thia-benzo[f]azulen-4-ylidene)piperidine-1-carboxylate 
• 1176736-68-7 4-(2-bromo-9,10-dihydro-1-thiabenzo[f]-azulen-4-ylidene)-1-methylpiperidine 
• 1176739-46-0 3-[4-piperidin-4-ylidene-4H-1-thiabenzo[f]azulen-2-yl]-propionic acid 
• 98-11-3 benzenesulfonic acid 
• 15574-96-6 pizotifen 

Relevant articles and documents

PROCESS FOR PRODUCING THIABENZOAZULENE-PROPIONIC ACID DERIVATIVE

Disclosed is a process for producing a thiabenzoazulene-propionic acid derivative which is useful as an active ingredient of an antihistaminic agent or the like. According to the producing process of the present invention, it is possible to produce a thiabenzoazulene-propionic acid derivative where the 2-position of the thiabenzoazulene skeleton is substituted with propionic acid. The thiabenzoazulene propionic-acid derivative thus synthesized has excellent antagonistic action to histamine H1 receptor and low intracerebral transmigration and, therefore, is useful as an active ingredient of the pharmaceutical composition such as an antihistaminic agent.