1459809-09-6

Basic information

• Product Name: 7,8-dihydroxy-N-(4-((4-(trifluoromethyl)phenyl)diazenyl)phenethyl)-4,5-dihydro-1H-benzo[c]azepine-2(3H)-carbothioamide
• Synonyms: 7,8-dihydroxy-N-(4-((4-(trifluoromethyl)phenyl)diazenyl)phenethyl)-4,5-dihydro-1H-benzo[c]azepine-2(3H)-carbothioamide
• CAS NO: 1459809-09-6
• Molecular Weight: 514.571
• Mol File: 1459809-09-6.mol

Chemical Properties

• CAS DataBase Reference: 7,8-dihydroxy-N-(4-((4-(trifluoromethyl)phenyl)diazenyl)phenethyl)-4,5-dihydro-1H-benzo[c]azepine-2(3H)-carbothioamide(CAS DataBase Reference)
• NIST Chemistry Reference: 7,8-dihydroxy-N-(4-((4-(trifluoromethyl)phenyl)diazenyl)phenethyl)-4,5-dihydro-1H-benzo[c]azepine-2(3H)-carbothioamide(1459809-09-6)
• EPA Substance Registry System: 7,8-dihydroxy-N-(4-((4-(trifluoromethyl)phenyl)diazenyl)phenethyl)-4,5-dihydro-1H-benzo[c]azepine-2(3H)-carbothioamide(1459809-09-6)

Safety Data

• Hazardous Substances Data: 1459809-09-6(Hazardous Substances Data)

Usage

Uses

AC 4 is a photoswitchable compound, which converts TRPV1 channels into photoreceptors.

Upstream product

• 253135-15-8 7-hydroxy-8-methoxy-2,3,4,5-tetrahydro-1H-2-benzazepine 
• 253135-14-7 2-benzyl-7-hydroxy-8-methoxy-2,3,4,5-tetrahydro-2-benzazepine 
• 253135-13-6 N-benzyl-3-(3-hydroxy-4-methoxyphenyl)propylamine 
• 253135-11-4 N-benzyl-3-(3-hydroxy-4-methoxyphenyl)propanamide 
• 1135-15-5 dihydroisoferulic acid 
• 129150-61-4 3-(3-hydroxy-4-methoxyphenyl)-propionic acid methyl ester 
• 97966-29-5 methyl (E)-3-(3-hydroxy-4-methoxyphenyl)-2-propenoate 
• 1459808-92-4 C₁₅H₁₄F₃N₃ 
• 1459808-91-3 tert-butyl 4-((4-(trifluoromethyl)phenyl)diazenyl)phenethylcarbamate 
• 621-59-0 isovanillin 
• 94838-59-2 tert-butyl 4-aminophenethylcarbamate 
• 13472-00-9 p-Aminophenethylamine 
• 1459808-93-5 1-(4-(2-isothiocyanatoethyl)phenyl)-2-(4-(trifluoromethyl)phenyl)diazene 

Relevant articles and documents

Optical control of TRPV1 channels

Controlling pain with light: TRPV1 channels mediate the response to noxious heat and can be activated by capsaicin, the major ingredient of chili pepper. Novel azobenzene photoswitches can be used for the optical control of TRPV1. One of these compounds antagonizes capsaicin in a light-dependent fashion, demonstrating that a photoswitchable antagonist and an agonist can be applied in concert to modulate ion channel activity. Copyright