slaframine

slaframine Suppliers list
Company Name: LEAP CHEM CO., LTD.
Tel: +86-852-30606658
Email: market18@leapchem.com
Products Intro: Product Name:SLAFRAMINE
CAS:20084-93-9
Package:1g; 5g; 25g; 1kg; 5kg; 25kg
Company Name: Chengdu Push Bio-Technology Co., Ltd.  
Tel: 18080489829
Email: 3004654993@qq.com
Products Intro: Product Name:(-)-Slaframine
CAS:20084-93-9
Purity:95% Package:5mg
Company Name: Hangzhou Bingochem Co., Ltd.  
Tel: 0571-87632989
Email: sales@bingochem.com
Products Intro: Product Name:0
CAS:20084-93-9
Purity:99% HPLC Package:1g; 5g; 25g; 1kg; 5kg; 25kg
slaframine Basic information
Product Name:slaframine
Synonyms:slaframine;(1S,8aα)-6β-Aminooctahydroindolizin-1β-ol acetate;1-Indolizinol, 6-aminooctahydro-, 1-acetate, (1S,6S,8aS)-;(-)-Slaframine
CAS:20084-93-9
MF:C10H18N2O2
MW:198.26
EINECS:
Product Categories:
Mol File:20084-93-9.mol
slaframine Structure
slaframine Chemical Properties
Boiling point 278.5±35.0 °C(Predicted)
density 1.15±0.1 g/cm3(Predicted)
pka10.11±0.40(Predicted)
Safety Information
MSDS Information
slaframine Usage And Synthesis
DescriptionCertain legume forages used for dairy cattle feeding stock have been known to produce excessive salivation when infested by Rhizoctonia legurninicola and this has been shown to be due to the presence of an indolizidine alkaloid, slaframine. The base is amorphous and also yields an amorphous dihydrochloride. The dipicrate, however, is crystalline, m.p. l83-4°C as is also the N-acetyl derivative, m.p. l43-6°C; [α]25D - 15.9° (c 5.0, EtOH). NMR and high-resolution mass spectrometry have shown that the earlier structure required revision to that given above, namely l-acetoxy-6-aminooctahydroindolizidine. The configuration has been demonstrated to be 1 S,6S,8aS-.
Uses(-)-Slaframine, is an indolizidine alkaloidal mycotoxin that generally causes salivation (slobbers) in most animals. It is usually produced by the fungus Rhizoctonia leguminicola.
DefinitionChEBI: An indolizidine alkaloid that is octahydroindolizine substituted by an amino group at position 6 and an acetyloxy group at position 1.
ReferencesRainey et al., Nature, 205, 203 (1965)
Aust, Broquist., ibid, 205, 204 (1965)
Aust, Broquist, Rinehart.,l. Arner. Chern. Soc., 88,2879 (1966)
Whitlock et al., Tetrahedron Lett., 3819 (1966)
Revised structure:
Gardiner et al., J. Arner. Chern. Soc., 90,5639 (1968)
slaframine Preparation Products And Raw materials
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