Moschamine

Base Information

Chemical Name:Moschamine
CAS No.:68573-23-9
Molecular Formula:C20H20N2O4
Molecular Weight:352.39
Hs Code.:
European Community (EC) Number:849-485-8
NSC Number:369502
UNII:2PP8322487
DSSTox Substance ID:DTXSID70172925
Nikkaji Number:J1.973.598B,J923.310E
Wikipedia:N-Feruloylserotonin
Wikidata:Q25099720
Metabolomics Workbench ID:45730
ChEMBL ID:CHEMBL564482
Mol file:68573-23-9.mol

Synonyms:moschamine;N-feruloylserotonin

Suppliers and Price of Moschamine

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

TRC
N-FeruloylSerotonin
250mg
$ 1455.00

Medical Isotopes, Inc.
N-FeruloylSerotonin
250 mg
$ 2200.00

Arctom
Moschamine ≥98%
5mg
$ 318.00

Total 15 raw suppliers

Chemical Property of Moschamine

Chemical Property:

Vapor Pressure:1.43E-20mmHg at 25°C
Melting Point:110-114 °C
Boiling Point:705.6°Cat760mmHg
PKA:9.78±0.35(Predicted)
Flash Point:380.5°C
PSA：94.58000
Density:1.338g/cm³
LogP:3.35070
Storage Temp.:Refrigerator
Solubility.:DMSO (Slightly), Methanol (Slightly)
XLogP3:3
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:352.14230712
Heavy Atom Count:26
Complexity:498

Purity/Quality:

≥98% ^*data from raw suppliers

N-FeruloylSerotonin ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CNC3=C2C=C(C=C3)O)O
Isomeric SMILES:COC1=C(C=CC(=C1)/C=C/C(=O)NCCC2=CNC3=C2C=C(C=C3)O)O
Uses N-Feruloylserotonin is a conjugated serotonin compound that has been identified as the antioxidative component from the seed of Carthamus tinctorius. N-Feruloylserotonin displayed protective effects on oxidative damage in rat pheochromocytoma cells.

Technology Process of Moschamine

There total 9 articles about Moschamine 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: 99.0%

: 50-67-9
3-(2-aminoethyl)-1H-indol-5-ol

: 1135-24-6,537-98-4
(E)-3-(4-hydroxy-3-methoxyphenyl)acrylic acid

: 68573-23-9,193224-24-7
(2E)-N-[2-(5-hydroxy-1H-indol-3-yl)ethyl]-3-(4-hydroxy-3-methoxyphenyl)-2-propenamide

Guidance literature:: With benzotriazol-1-ol; dicyclohexyl-carbodiimide;
DOI:10.3987/COM-98-8156

Reference yield: 69.2%

: 68573-23-9,193224-24-7
(2E)-N-[2-(5-hydroxy-1H-indol-3-yl)ethyl]-3-(4-hydroxy-3-methoxyphenyl)-2-propenamide

Guidance literature:

Reference yield: 65.6%

: 1135-24-6,537-98-4
(E)-3-(4-hydroxy-3-methoxyphenyl)acrylic acid

: 153-98-0,21591-86-6
serotonin hydrochloride

: 68573-23-9,193224-24-7
(2E)-N-[2-(5-hydroxy-1H-indol-3-yl)ethyl]-3-(4-hydroxy-3-methoxyphenyl)-2-propenamide

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In dichloromethane; N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1021/jf060254p