Cinnamoyl tryptamine

Base Information

Chemical Name:Cinnamoyl tryptamine
CAS No.:212707-61-4
Molecular Formula:C19H18N2O
Molecular Weight:290.365
Hs Code.:
UNII:XY7RW8O14Q
Nikkaji Number:J1.078.170A
Wikidata:Q27294056
ChEMBL ID:CHEMBL520706
Mol file:212707-61-4.mol

Synonyms:212707-61-4;Cinnamoyl tryptamine;trans-N-[2-(3-Indolyl)ethyl]cinnamamide;Melaeser;XY7RW8O14Q;Cinnamoyl tryptamine [INCI];CHEMBL520706;(E)-N-[2-(1H-indol-3-yl)ethyl]-3-phenylprop-2-enamide;N-(2-(1H-indol-3-yl)ethyl)cinnamamide;2-Propenamide, N-(2-(1H-indol-3-yl)ethyl)-3-phenyl-, (2E)-;MFCD00170475;WAY-300015;UNII-XY7RW8O14Q;MLS001143325;HMS2778F06;74582-72-2;AC8199;BDBM50245092;STK530883;AKOS005463454;NCGC00311159-01;AC-29782;BAS 00337757;SMR000473160;CS-0449540;N-(2-indol-3-ylethyl)-3-phenylprop-2-enamide;AB00894236-05;A924426;Q27294056;(2E)-N-[2-(1H-indol-3-yl)ethyl]-3-phenylacrylamide;(2E)-N-[2-(1H-indol-3-yl)ethyl]-3-phenylprop-2-enamide

Suppliers and Price of Cinnamoyl tryptamine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 5 raw suppliers

Chemical Property of Cinnamoyl tryptamine

Chemical Property:

XLogP3:3.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:5
Exact Mass:290.141913202
Heavy Atom Count:22
Complexity:387

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C=CC(=O)NCCC2=CNC3=CC=CC=C32
Isomeric SMILES:C1=CC=C(C=C1)/C=C/C(=O)NCCC2=CNC3=CC=CC=C32

Technology Process of Cinnamoyl tryptamine

There total 6 articles about Cinnamoyl tryptamine 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: 83.0%

: 61-54-1
tryptamine

: 140-10-3
(E)-3-phenylacrylic acid

: 212707-61-4
(2E)-N-[2-(1H-indol-3-yl)ethyl]-3-phenylprop-2-enamide

Guidance literature:: (E)-3-phenylacrylic acid; With tris(2,2,2-trifluoroethyl) borate; In acetonitrile; at 20 ℃; for 0.166667h; Inert atmosphere; Sealed tube; Green chemistry;

tryptamine; In acetonitrile; at 100 ℃; for 24h; Inert atmosphere; Sealed tube; Green chemistry;
DOI:10.1016/j.ejps.2018.10.028

Reference yield: 77.0%

: 61-54-1
tryptamine

: 102-92-1,17082-09-6
Cinnamoyl chloride

: 212707-61-4
(2E)-N-[2-(1H-indol-3-yl)ethyl]-3-phenylprop-2-enamide

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 1h;
DOI:10.1039/c8gc01697f

Reference yield: 70.0%

: 61-54-1
tryptamine

: 17719-70-9,24968-99-8
(E)-vinyl cinnamate

: 212707-61-4
(2E)-N-[2-(1H-indol-3-yl)ethyl]-3-phenylprop-2-enamide

Guidance literature:: With immobilized onto glyoxyl-agarose beads acyl transferase from Mycobacterium smegmatis; In toluene; at 28 ℃; for 0.25h; Enzymatic reaction;
DOI:10.1016/j.tetlet.2021.153453