APOATROPINE

Base Information

Chemical Name:APOATROPINE
CAS No.:500-55-0
Deprecated CAS:78887-65-7
Molecular Formula:C17H21 N O2
Molecular Weight:271.359
Hs Code.:2933990090
European Community (EC) Number:207-906-7
UNII:3B4C10J0BP
DSSTox Substance ID:DTXSID801023633
Metabolomics Workbench ID:67797
Nikkaji Number:J12.242D
Wikidata:Q105310195,Q105310199
Wikipedia:Apoatropine
Mol file:500-55-0.mol

Synonyms:1aH,5aH-Tropan-3a-ol, atropate (ester) (8CI); Apoatropine (6CI,7CI); Benzeneacetic acid, a-methylene-,8-methyl-8-azabicyclo[3.2.1]oct-3-yl ester, endo-; Apoatropin; Apohyoscyamin;Apohyoscyamine; Atropamin; Atropamine; Atropyltropeine

Suppliers and Price of APOATROPINE

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

Medical Isotopes, Inc.
Apoatropine
10 mg
$ 490.00

Arctom
Apoatropine ≥98%
5mg
$ 468.00

American Custom Chemicals Corporation
BELLADONNINE 95.00%
5MG
$ 495.48

Total 21 raw suppliers

Chemical Property of APOATROPINE

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Melting Point:62°
Refractive Index:1.5675 (estimate)
Boiling Point:389.1°Cat760mmHg
PKA:10.01±0.40(Predicted)
Flash Point:136.5°C
PSA：29.54000
Density:1.13g/cm³
LogP:2.80610
XLogP3:3.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:271.157228913
Heavy Atom Count:20
Complexity:373

Purity/Quality:

99%, ^*data from raw suppliers

Apoatropine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Statements: 26/28
Safety Statements: 25-45

MSDS Files:

Useful:

Canonical SMILES:CN1C2CCC1CC(C2)OC(=O)C(=C)C3=CC=CC=C3
Isomeric SMILES:CN1[C@@H]2CC[C@H]1CC(C2)OC(=O)C(=C)C3=CC=CC=C3
Uses Apoatropine is an alkaloid derivative with the potential to be an antibacterial.

Technology Process of APOATROPINE

There total 18 articles about APOATROPINE 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: 58.0%

: 51-55-8
Atropine

: 500-55-0
apoatropine

Guidance literature:: Atropine; With copper(l) chloride; diisopropyl-carbodiimide; at 60 ℃; for 1h; Sealed tube; Microwave irradiation;

With copper (II)-fluoride; In water; at 100 ℃; for 24h; Microwave irradiation;
DOI:10.1002/anie.202001015