3-Iodothyronamine

Base Information

• Chemical Name: 3-Iodothyronamine
• CAS No.: 712349-95-6
• Molecular Formula: C₁₄H₁₄INO₂
• Molecular Weight: 355.175
• European Community (EC) Number: 685-805-0
• UNII: VMM45J7F4L
• DSSTox Substance ID: DTXSID80433256
• Nikkaji Number: J2.051.793J
• Wikipedia: 3-Iodothyronamine
• Wikidata: Q2815997
• Metabolomics Workbench ID: 121145
• ChEMBL ID: CHEMBL1182312
• Mol file: 712349-95-6.mol

Synonyms:3-iodothyronamine;T(1)AM cpd

Chemical Property of 3-Iodothyronamine

Chemical Property:

• PSA: 55.48000
• LogP: 4.79260
• XLogP3: 3.1
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 355.00693
• Heavy Atom Count: 18
• Complexity: 244

Purity/Quality:

98% ^*data from raw suppliers

3-Iodothyronamine-ethylamino-1,1,2,2-d4HCl >=98% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=CC=C1O)OC2=C(C=C(C=C2)CCN)I

Technology Process of 3-Iodothyronamine

There total 1 articles about 3-Iodothyronamine 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:

3,5-diiodothyronamine trifluoroacetate → 3-Iodothyronamine (712349-95-6)

Guidance literature:

With sodium tetrahydroborate; DL-dithiothreitol; Naphthalene-1,8-diselenol; In aq. phosphate buffer; acetonitrile; at 37 ℃; pH=7; Reagent/catalyst; pH-value; regioselective reaction; Kinetics;

DOI:10.1039/c6ob01375a

Refernces