103544-23-6

Basic information

• Product Name: 3-amino-N,N-dipropylbenzeneethanamine
• Synonyms: 3-amino-N,N-dipropylbenzeneethanamine
• CAS NO: 103544-23-6
• Molecular Weight: 0
• Mol File: 103544-23-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-amino-N,N-dipropylbenzeneethanamine(CAS DataBase Reference)
• NIST Chemistry Reference: 3-amino-N,N-dipropylbenzeneethanamine(103544-23-6)
• EPA Substance Registry System: 3-amino-N,N-dipropylbenzeneethanamine(103544-23-6)

Safety Data

• Hazardous Substances Data: 103544-23-6(Hazardous Substances Data)

Upstream product

• 69628-97-3 toluene-4-sulfonic acid 2-(3-nitrophenyl)ethyl ester 
• 142-84-7 di-n-propylamine 
• 52022-77-2 2-(3-nitrophenyl)ethanol 
• 97351-97-8 N,N-di-n-propyl-2-(3-nitrophenyl)acetamide 
• 1877-73-2 3-nitro-benzeneacetic acid 
• 38411-41-5 (3-nitrophenyl)acetyl chloride 
• 122520-07-4 N,N-di-n-propyl-2-(3-aminophenyl)acetamide 
• 97351-96-7 3-nitro-N,N-dipropylbenzeneethanamine 

Downstream Products

• 103544-35-0 1-[3-(2-N,N-di-n-propylaminoethyl)phenyl]-3-methylurea 
• 97351-98-9 N-<3-<2-(dipropylamino)ethyl>phenyl>acetamide 

Relevant articles and documents

Synthesis and Evaluation of N,N-Di-n-propyltetrahydrobenzindol-7-amine and Related Congeners as Dopaminergic Agonists

An evaluation of 6-indole (4), its rigid analogue N,N-di-n-propyl-5,6,7,8-tetrahydrobenzindol-7-amine (5), and some related congeners, for ability to suppress serum prolactin in reserpinized rats, revealed modest biological a

4--2(3H)-indolone: A Prejunctional Dopamine Receptor Agonist

4--2(3H)-indolone (1c) (SK and F 101468) is a potent and selective prejunctional dopamine receptor agonist.It caused a dose-related inhibition of the constrictor response to electrical stimulation in the isolated perfused rabbit ear artery (EC50 = 100 nM), and this response was antagonized by (S)-sulpiride (KB = 7 nM).Compound 1c did not stimulate or block dopamine-sensitive adenylate cyclase and did not produce stimulation of the central nervous system in rats.It was prepared from (2-methyl-3-nitrophenyl)acetic acid in a multistep sequence based on the Reissert indole synthesis.