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Anisodine

Base Information Edit
  • Chemical Name:Anisodine
  • CAS No.:52646-92-1
  • Molecular Formula:C17H21NO5
  • Molecular Weight:319.35
  • Hs Code.:
  • UNII:Z75256J75J
  • ChEMBL ID:CHEMBL5095784
  • DSSTox Substance ID:DTXSID20967080
  • Nikkaji Number:J39.182D
  • Wikidata:Q76421770
  • Wikipedia:Anisodine
  • Mol file:52646-92-1.mol
Anisodine

Synonyms:anisodine;anisodine hydrobromide;anisodine hydrochloride

Suppliers and Price of Anisodine
Supply Marketing:Edit
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
  • AvaChem
  • Anisodine
  • 10mg
  • $ 590.00
  • AvaChem
  • Anisodine
  • 5mg
  • $ 390.00
Total 3 raw suppliers
Chemical Property of Anisodine Edit
Chemical Property:
  • Boiling Point:495°Cat760mmHg 
  • Flash Point:253.2°C 
  • PSA:82.53000 
  • Density:1.39g/cm3 
  • LogP:-0.04000 
  • XLogP3:0.6
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:5
  • Exact Mass:319.14197277
  • Heavy Atom Count:23
  • Complexity:462
Purity/Quality:

98%Min *data from raw suppliers

Anisodine *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CN1C2CC(CC1C3C2O3)OC(=O)C(CO)(C4=CC=CC=C4)O
  • Isomeric SMILES:CN1[C@@H]2CC(C[C@H]1[C@H]3[C@@H]2O3)OC(=O)[C@@](CO)(C4=CC=CC=C4)O
  • Description Anisodine is isolated from the roots of the plant Solanaceae Anisodus tanguticus (Maxim.) Pasch. (Scopolia tangutica Maxim.), which has a common name of Zhang-Liu-Shen, growing at the plateau with an altitude of 1700–4300?m and richly distributed in Tibet, Sichuan, Qinghai, Gansu, and other provinces in China.
  • Physical properties Appearance: white crystals or crystalline powder. Flash point: 253.2?°C. Melting point: 126–128? °C (acetone-H2O), 190–192? °C (95% ethanol), and 197–200? °C (absolute ethanol). MS m/e (%): 319(51), 154(14), 138(100), 96(5), 95(5), 94(36), 97(15), 96(5), 42(15), 137(25), and 119(23).
  • Indications Anisodine hydrobromide is recorded in the second volume of national standards for chemical drugs of the People’s Republic of China. The formulation consists of injection and tablet. It is used clinically for treatment of migraine, retinal vascular spasm, ischemic lesions, shrinking of the optic nerve, retina, and choroid, etc. It could improve the functional recovery after acute paralysis induced by inflammation of the nervous system and cerebrovascular disease, paralysis agitants, and carbon monoxideinduced toxic encephalopathy. It was also used for intravenous combined anesthesia, organophosphorus poisoning, bronchitis, asthma, and prevention and treatment of seasickness.
  • Clinical Use In the past, anisodine was mainly used in the treatment of various diseases of the central nervous system. It had a certain therapeutic effect on patients with very low vision and deservesclinical application . When used for ischemic optic neuropathy treatment, anisodine significantly promoted the recovery of the visual field, with the effective rate as high as 82.14% compared with conventional therapeutic regimen using corticosteroids combined with vasodilators, thrombolytic agents, vitamins, and antibiotics.
Technology Process of Anisodine

There total 5 articles about Anisodine 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:
Guidance literature:
Multi-step reaction with 2 steps
1: 78.9 percent / V2O5; aq. H2O2 / acetonitrile / 8 h / 45 °C
2: AD-mix α / 2-methyl-propan-2-ol; H2O / 24 h / 0 °C
With AD-mix-α; dihydrogen peroxide; vanadia; In water; acetonitrile; tert-butyl alcohol; 2: Sharpless dihydroxylation;
DOI:10.1016/j.ejmech.2005.12.001
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