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Heliotridine is a necine base alkaloid derived from plants, which is known for its hepatotoxic effects and its ability to inhibit mitochondrial metabolism. HELIOTRIDINE has been found to have various applications in different industries due to its unique properties.

520-63-8

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520-63-8 Usage

Uses

Used in Pharmaceutical Industry:
Heliotridine is used as a pharmaceutical compound for its hepatotoxic effects and its ability to inhibit mitochondrial metabolism. This makes it a potential candidate for the development of drugs targeting specific conditions related to liver function and cellular metabolism.
Used in Research and Development:
In the field of research and development, Heliotridine is utilized as a chemical compound for studying the effects of hepatotoxicity and mitochondrial metabolism inhibition. This helps scientists to better understand the underlying mechanisms and develop new therapeutic strategies for various diseases.
Used in Toxicology Studies:
Heliotridine is also used in toxicology studies to investigate the effects of hepatotoxic substances on the liver and other organs. This helps in assessing the safety and potential risks associated with the use of certain compounds in pharmaceuticals and other applications.

Check Digit Verification of cas no

The CAS Registry Mumber 520-63-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,2 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 520-63:
(5*5)+(4*2)+(3*0)+(2*6)+(1*3)=48
48 % 10 = 8
So 520-63-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H13NO2/c10-5-6-1-3-9-4-2-7(11)8(6)9/h1,7-8,10-11H,2-5H2/t7-,8+/m0/s1

520-63-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-Pyrrolizine-7-methanol,2,3,5,7a-tetrahydro- 1-hydroxy-,(1S,7aR)-

1.2 Other means of identification

Product number -
Other names (1S,7aR)-2,3,5,7a-Tetrahydro-1-hydroxy-1H-pyrrolizine-7-methanol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:520-63-8 SDS

520-63-8Relevant academic research and scientific papers

Expedient pyrrolizidine synthesis by propargylsilane addition to N-acyliminium ions followed by gold-catalyzed α-allenyl amide cyclization

Breman, Arjen C.,Dijkink, Jan,Van Maarseveen, Jan H.,Kinderman, Sape S.,Hiemstra, Henk

supporting information; experimental part, p. 6327 - 6330 (2009/12/24)

(Chemical Equation Presented) A reaction sequence, involving the addition of (substituted) propargylsilanes to lactam-derived N-acyliminium ions followed by gold-catalyzed cyclization of the resulting α-allenyl amide, is applied in expedient syntheses of

Reactions of iminium ions with Michael acceptors through a Morita-Baylis-Hillman-type reaction: Enantiocontrol and applications in synthesis

Myers, Eddie L.,De Vries, Johannes G.,Aggarwal, Varinder K.

, p. 1893 - 1896 (2008/03/12)

(Chemical Equation Presented) All adducts one way: Iminium ions, generated in situ from the corresponding N,O-acetals, can be used as electrophiles in a Morita-Baylis-Hillman-type reaction with a wide range of Michael acceptors (enones, enals, S- and O-acrylates). The reaction has been rendered asymmetric using sulfide 1 (see scheme; DBU = 1,8-diazabicyclo[5.4.0]undec-7-ene, TMSOTf=trimethylsilyl trifluoromethanesulfonate).

Isoechinatine, a pyrrolizidine alkaloid from Cynoglossum furcatum

Ravikumar,Lakshmanan

, p. 406 - 409 (2007/10/03)

The pyrrolizidine alkaloids of Cynoglossum furcatum have been isolated and characterized. They are isoechinatine 1, a new pyrrolizidine ester alkaloid, echinatine, neocoramandaline and a free necine heliotridine. Isoechinatine is formulated as 9-(O)-(+)-viridiflorylheliotridine. 3-Hydroxy 6-methylpyridine has also been isolated and characterized.

Intramolecular Allylstannane Cyclizations in Alkaloid Synthesis: Applications to Pyrrolizidine Alkaloids

Keck, Gary E.,Cressman, Erik N. K.,Enholm, Eric J.

, p. 4345 - 4349 (2007/10/02)

Syntheses of (+/-)-isoretronecanol, (+/-)-supinidine, (-)-dihydroxyheliotridane, and (+)-heliotridine are detailed.The key step in each case involves an intramolecular acyliminium ion cyclization onto a suitably positioned allylstannane for construction o

Pyrrolizidine Alkaloid Biosynthesis. Synthesis of 3H-Labelled Trachelanthamidine and Isoretronecanol and their Incorporation into Three Pyrrolizidine Bases (Necines)

Kunec, Ellen K.,Robins, David J.

, p. 1437 - 1441 (2007/10/02)

(+/-)-Isoretronecanol (22) and (+/-)-trachelanthamidine (24) were prepared by 1,3-dipolar cycloaddition of N-formylproline with ethyl propiolate followed by reduction steps.These 3H-labelled 1-hydroxymethylpyrrolizidines together with putrescine were fed to Senecio isatideus which produces retrorsine (1); S. pleistocephalus which yields rosmarinine (8); and Cynoglossum officinale which affords echinatine (5).The double labelling experiments demonstrated that isoretronecanol is incorporated much more efficiently into rosmarinine than into retrorsine or echinatine, whereas trachelanthamidine is a much more efficient precursor for retrorsine and echinatine.Base hydrolysis of retrorsine and echinatine labelled with trachelanthamidine and of rosmarinine labelled with isoretronecanol established that most of the 3H-label was in the base portions, retronecine (2), heliotridine (6), and rosmarinecine (9), respectively.Further degradation of retronecine and rosmarinecine showed that most of the radioactivity was confined to the β-alanine (4) portion.The biosynthetic pathways to isoretronecanol and trachelanthamidine apparently diverge prior to the formation of these 1-hydroxymethylpyrrolizidines, probably during the cyclisation of an immonium ion (14) to form the 1-formylpyrrolizidines (15) and (17).

AN IMPROVED SYNTHESIS OF (+)-HELIOTRIDINE

Kano, Shinzo,Yuasa, Yoko,Shibuya, Shiroshi

, p. 253 - 256 (2007/10/02)

An alternative synthesis of (+)-heliotridine was achieved from 7-hydroxy-1-methylene-hexahydro-3H-pyrrolizin-5-one,through conversion of exo-methylene to allylic alcohol part.

Pyrrolizidine Alkaloid Analogues. Synthesis of 11-Membered Macrocyclic Diesters of (+)-Heliotridine

Hagan, Desmond B.,Robins, David J.

, p. 1165 - 1168 (2007/10/02)

The first synthesis of macrocyclic diesters incorporating (+)-heliotridine has been achieved.Treatment of (+)-heliotridine (1) with different glutaric anhydride derivatives produced mainly the corresponding 9-monoesters of heliotridine.Lactonisation was carried out after formation of the pyridine-2-thiol esters to give a range of 11-membered macrocyclic diesters of heliotridine.The structures of these new pyrrolizidine alkaloid analogues were established by comparison of their (1)H n.m.r. and mass spectra with those of natural macrocyclic pyrrolizidine alkaloids.Attempts to make 10-membered macrocyclic diesters of heliotridine were unsuccessful.

THE SYNTHESIS OF HELIOTRIDINE AND RELATED ALKALOIDS

Glinski, Jan A.,Zalkow, Leon H.

, p. 2857 - 2860 (2007/10/02)

An efficient synthesis of heliotridine from readily available retronecine was accomplished by nucleophilic displacement of the 7-mesylate, in the 7-mesyl-9-benzoate of retronecine with various cesium carboxylates in DMF, followed by hydrolysis.The synthet

FREE RADICAL CYCLIZATIONS IN ALKALOID SYNTHESIS: (+)-HELIOTRIDINE AND (+)-HASTANECINE

Choi, Joong-Kwon,Hart, David J.

, p. 3959 - 3972 (2007/10/02)

Treatment of phenylthiolactams 5a-5f with tri-n-butyltin hydride and AIBN affords mixtures of reduction and cyclization products.Cyclization products partition between indolizidinones and pyrrolizidinones depending on the terminal alkyne substituent.When

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