147918-24-9

Basic information

• Product Name: N,O-Dibenzyl Serotonin
• Synonyms: N,O-Dibenzyl Serotonin
• CAS NO: 147918-24-9
• Molecular Formula: C₂₄H₂₄N₂O
• Molecular Weight: 355.45222
• Product Categories: Aromatics, Heterocycles, Pharmaceuticals, Intermediates & Fine Chemicals, Neurochemicals
• Mol File: 147918-24-9.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• Solubility: Ethyl Acetate, Methanol
• CAS DataBase Reference: N,O-Dibenzyl Serotonin(CAS DataBase Reference)
• NIST Chemistry Reference: N,O-Dibenzyl Serotonin(147918-24-9)
• EPA Substance Registry System: N,O-Dibenzyl Serotonin(147918-24-9)

Safety Data

• Hazardous Substances Data: 147918-24-9(Hazardous Substances Data)

Usage

Chemical Properties

Pale Yellow Oil

Uses

Protected Serotonin (S274980), a monoamine neurotransmitter.

Upstream product

• 102754-41-6 N-Benzyl-2-<5-(benzyloxy)-3-indolyl>glyoxylamid 
• 1215-59-4 5-benzyloxy-1H-indole 
• 22424-61-9 2-[5-(benzyloxy)-1H-indol-3-yl]-2-oxoacetyl chloride 
• 104-63-2 N-Benzylethanolamine 

Downstream Products

• 50-67-9 3-(2-aminoethyl)-1H-indol-5-ol 
• 147918-28-3 6-Benzyloxy-1-(2-<(2,4,10-Trioxatricyclo<3.3.1.1^3,7>dec-3-yl)ethyl>)-9H-pyrido<3,4-b>indol 
• 147918-26-1 2-Benzyl-6-(benzyloxy)-1-(2-<(2,4,10-trioxatricyclo<3.3.1.1^3,7>dec-3-yl)ethyl>)-1,2,3,4-tetrahydro-9H-pyrido<3,4-b>indol 

Relevant articles and documents

Observations concerning the synthesis of tryptamine homologues and branched tryptamine derivatives via the borrowing hydrogen process: Synthesis of psilocin, bufotenin, and serotonin

Observations concerning the synthesis of substituted tryptamine derivatives starting from indoles and 1,n-amino alcohols via the borrowing hydrogen process are discussed. This catalytic, single-step, and modular approach to tryptamines and homotryptamines allows the synthesis of branched and nonbranched tryptamines as well as tryptamine-based natural products such as psilocin, bufotenin, and serotonin.