Tdo-HT

Base Information

• Chemical Name: Tdo-HT
• CAS No.: 118230-91-4
• Molecular Formula: C₃₀H₃₀N₆O₄
• Molecular Weight: 538.606
• DSSTox Substance ID: DTXSID10152044
• Wikidata: Q83018614
• Mol file: 118230-91-4.mol

Synonyms:4-(7'-(tryptamine-4,5-dione))-2,4''-bis-5-hydroxytryptamine

Chemical Property of Tdo-HT

Chemical Property:

• Vapor Pressure: 0mmHg at 25°C
• Boiling Point: 945.2°Cat760mmHg
• PKA: 8.69±0.50(Predicted)
• Flash Point: 525.5°C
• PSA: 200.03000
• Density: 1.497g/cm³
• LogP: 4.85710
• XLogP3: 0.7
• Hydrogen Bond Donor Count: 8
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 8
• Exact Mass: 538.23285346
• Heavy Atom Count: 40
• Complexity: 993

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=C(C2=C1NC=C2CCN)C3=C(C4=C(N3)C=CC(=C4C5=CC(=O)C(=O)C6=C5NC=C6CCN)O)CCN)O

Technology Process of Tdo-HT

There total 1 articles about Tdo-HT which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

serotonin hydrochloride (153-98-0,21591-86-6) → 5,5′-dihydroxy-4,4′-bitryptamine (108535-01-9) + 3-(2-aminoethyl)-3-<3'-(2-aminoethyl)-5'-hydroxyindol-4'-yl>-5-hydroxyindolenine (114564-02-2) + 3-(2-aminoethyl)-3-<3'-(2-aminoethyl)-5'-hydroxyindol-4'-yl>indolenine-5,6-dione (120666-68-4) + 4-[3-(2-Amino-ethyl)-5-hydroxy-1H-indol-4-yl]-quinolin-6-ol + 7,7'-Bi-(5-hydroxytryptamine-4-one) (118230-89-0) + 4-<7'-(tryptamine-4,5-dione)>-2,4'-bi-5-hydroxytryptamine (118230-91-4)

Guidance literature:

With hydrogenchloride; Product distribution; electrooxidation, 0.530 V; electrochemical transformations of 5-hydroxytryptamine and its products;

DOI:10.1002/jps.2600771102

upstream raw materials:

serotonin hydrochloride

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