Indorenate

Base Information

Chemical Name:Indorenate
CAS No.:73758-06-2
Molecular Formula:C₁₃H₁₆N₂O₃
Molecular Weight:248.282
Hs Code.:
UNII:AV9L041QA4
DSSTox Substance ID:DTXSID2048400
Nikkaji Number:J363.352G,J363.353E
Wikipedia:Indorenate
Wikidata:Q6026626
NCI Thesaurus Code:C83802
ChEMBL ID:CHEMBL414636
Mol file:73758-06-2.mol

Synonyms:5-methoxytryptamine beta-methylcarboxylate;indorenate;TR 3369;TR-3369;TR3369

Suppliers and Price of Indorenate

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

American Custom Chemicals Corporation
INDORENATE 95.00%
5MG
$ 505.40

Total 3 raw suppliers

Chemical Property of Indorenate

Chemical Property:

Vapor Pressure:4.89E-08mmHg at 25°C
Boiling Point:442.8°C at 760 mmHg
Flash Point:221.6°C
PSA：77.34000
Density:1.243g/cm³
LogP:2.09210
XLogP3:0.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:248.11609238
Heavy Atom Count:18
Complexity:298

Purity/Quality:

99% ^*data from raw suppliers

INDORENATE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC2=C(C=C1)NC=C2C(CN)C(=O)OC

Technology Process of Indorenate

There total 4 articles about Indorenate 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:

: 73139-80-7
ethyl α-cyano-α-(1-carbethoxy-5-methoxy-3-indolyl)acetate

: 73758-06-2
Indorenate

Guidance literature:: Multi-step reaction with 3 steps

1: 56 percent / H₂ / Raney Ni (W-4) / 2585.7 Torr

2: 64 percent / 10 N NaOH / 8 h / Heating

3: SOCl₂ / 18 h / Ambient temperature

With sodium hydroxide; thionyl chloride; hydrogen; Raney Ni (W-4);
DOI:10.1021/jm00348a022

Reference yield:

: 73139-81-8
ethyl 3-acetamido-2-(1-carbethoxy-5-methoxy-3-indolyl)propionate

: 73758-06-2
Indorenate

Guidance literature:: Multi-step reaction with 2 steps

1: 64 percent / 10 N NaOH / 8 h / Heating

2: SOCl₂ / 18 h / Ambient temperature

With sodium hydroxide; thionyl chloride;
DOI:10.1021/jm00348a022