Adrenoglomerulotropin

Base Information

Chemical Name:Adrenoglomerulotropin
CAS No.:1210-56-6
Molecular Formula:C13H16 N2 O
Molecular Weight:216.283
Hs Code.:2933990090
UNII:U18P8J9O2I
DSSTox Substance ID:DTXSID20871835
Nikkaji Number:J7.456J
Wikipedia:6-MeO-THH
Wikidata:Q4057960
ChEMBL ID:CHEMBL221811
Mol file:1210-56-6.mol

Synonyms:1-Me-6-MTHBC;1-methyl-6-methoxy-tetrahydro-beta-carboline;6-methoxy-1-methyl-1,2,3,4-tetrahydro-beta-carboline;adrenoglomerulotropin

Suppliers and Price of Adrenoglomerulotropin

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
MMTC
1mg
$ 55.00

American Custom Chemicals Corporation
MMTC 95.00%
5MG
$ 499.13

Total 11 raw suppliers

Chemical Property of Adrenoglomerulotropin

Chemical Property:

Vapor Pressure:1.4E-06mmHg at 25°C
Melting Point:150-151°
Refractive Index:1.6450 (estimate)
Boiling Point:399.2°Cat760mmHg
PKA:17.51±0.40(Predicted)
Flash Point:195.2°C
PSA：37.05000
Density:1.145g/cm³
LogP:2.71200
XLogP3:1.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:216.126263138
Heavy Atom Count:16
Complexity:258

Purity/Quality:

98%min ^*data from raw suppliers

MMTC ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1C2=C(CCN1)C3=C(N2)C=CC(=C3)OC
Uses MMTC is an analog of pinolin found to increase the concentration of plasma aldosterone and inhibit the uptake of seratonin.

Technology Process of Adrenoglomerulotropin

There total 5 articles about Adrenoglomerulotropin 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: 80.0%

: 608-07-1
2-(5-methoxyindol-3-yl)ethylamine

: 75-07-0,9002-91-9
acetaldehyde

: 1210-56-6
6-methoxy-1-methyl-1,2,3,4-tetrahydro-β-carboline

Guidance literature:: 2-(5-methoxyindol-3-yl)ethylamine; With trifluoroacetic acid; In dichloromethane; at 0 ℃; for 0.5h;

acetaldehyde; In dichloromethane; at 20 ℃; for 24h;
DOI:10.1016/j.bioorg.2020.103844