374808-69-2

Basic information

• Product Name: thioacetic acid S-[10-(4-{3-[(4-(2-benzhydryloxyethyl)piperazin-1-yl)propyl]phenyl}carbamoyl)decyl] ester
• Synonyms: thioacetic acid S-[10-(4-{3-[(4-(2-benzhydryloxyethyl)piperazin-1-yl)propyl]phenyl}carbamoyl)decyl] ester
• CAS NO: 374808-69-2
• Molecular Weight: 671.988
• Mol File: 374808-69-2.mol

Chemical Properties

• CAS DataBase Reference: thioacetic acid S-[10-(4-{3-[(4-(2-benzhydryloxyethyl)piperazin-1-yl)propyl]phenyl}carbamoyl)decyl] ester(CAS DataBase Reference)
• NIST Chemistry Reference: thioacetic acid S-[10-(4-{3-[(4-(2-benzhydryloxyethyl)piperazin-1-yl)propyl]phenyl}carbamoyl)decyl] ester(374808-69-2)
• EPA Substance Registry System: thioacetic acid S-[10-(4-{3-[(4-(2-benzhydryloxyethyl)piperazin-1-yl)propyl]phenyl}carbamoyl)decyl] ester(374808-69-2)

Safety Data

• Hazardous Substances Data: 374808-69-2(Hazardous Substances Data)

Upstream product

• 374808-68-1 11-bromoundecanoic acid (4-{3-[4-(2-benzhydryloxyethyl)piperazin-1-yl]propyl}phenyl)amide 
• 10387-40-3 potassium thioacetate 
• 374808-04-5 1-[2-[bisphenylmethoxy]ethyl]-4-(3-(4-nitrophenyl)-1-oxopropyl)piperazine 
• 127139-25-7 1-[2-[bis(phenyl)methoxy]ethyl]-4-(3-(4-aminophenyl)propyl)piperazine 
• 16642-79-8 3-(4-nitrophenyl)propionic acid 
• 15949-84-5 11-bromoundecanoyl chloride 
• 2834-05-1 11-bromoundecanoic acid 

Relevant articles and documents

The design and synthesis of novel derivatives of the dopamine uptake inhibitors GBR 12909 and GBR 12935. High-affinity dopaminergic ligands for conjugation with highly fluorescent cadmium selenide/zinc sulfide core/shell nanocrystals

There is a growing demand for compounds with very high affinities for the dopamine transporter protein (DAT) that can be conjugated to fluorescent markers such as cadmium selenide/zinc sulfide core/shell nanocrystals. This paper describes the design and synthesis of two derivatives of the DAT antagonists GBR 12935 and GBR 12909. These compounds have a high biological affinity for DAT and may be conjugated to nanocrystals via a thiol linkage without a significant reduction in their biological activity. Such conjugates may be used in fluorescent imaging studies.