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3(2H)-Indolizinone,hexahydro-5,7-dimethyl-,(5R,7S,8aR)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

727985-47-9

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727985-47-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 727985-47-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,7,9,8 and 5 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 727985-47:
(8*7)+(7*2)+(6*7)+(5*9)+(4*8)+(3*5)+(2*4)+(1*7)=219
219 % 10 = 9
So 727985-47-9 is a valid CAS Registry Number.

727985-47-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (5R,7S,8aR)-(-)-5,7-dimethylindolizidine-3-one

1.2 Other means of identification

Product number -
Other names (5R,7S,8aR)-5,7-dimethyl-indolizidin-3-one

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:727985-47-9 SDS

727985-47-9Downstream Products

727985-47-9Relevant academic research and scientific papers

Stereocontrolled synthesis of substituted chiral piperidines viaone-pot asymmetric 6π-azaelectrocyclization: Asymmetric syntheses of(-)-dendroprimine, (+)-7-epidendroprimine, (+)-5-epidendroprimine, and (+)-5,7-epidendroprimine

Kobayashi, Toyoharu,Hasegawa, Futoshi,Hirose, Yoshikatsu,Tanaka, Katsunori,Mori, Hajime,Katsumura, Shigeo

, p. 1812 - 1832 (2012/04/04)

The asymmetric one-pot 6π-azaelectrocyclization of alkenyl vinyl stannane, ethyl (Z)-2-iodo-4-oxobutenoate, and (-)-7-isopropyl-cis-aminoindanol in the presence of a Pd(0) catalyst stereoselectively produced the tetracyclic aminoacetal compounds, resultin

Synthesis of 2,4,6-trisubstituted chiral piperidines and (-)-dendroprimine by one-pot asymmetric azaelectrocyclization protocol

Kobayashi, Toyoharu,Hasegawa, Futoshi,Tanaka, Katsunori,Katsumura, Shigeo

, p. 3813 - 3816 (2007/10/03)

Stereocontrolled synthesis of 2,4,6-trisubstituted piperidine diastereomers has been realized from common intermediates, obtained by a one-pot azaelectrocyclization protocol. Based on the method, the asymmetric synthesis of an indolizidine alkaloid, (-)-d

Enantioselective synthesis of (-)-dendroprimine and isomers

De Saboulin Bollena, Axelle,Gelas-Mialhe, Yvonne,Gramain, Jean-Claude,Perret, Anne,Remuson, Roland

, p. 1029 - 1031 (2007/10/03)

An enantioselective and diastereoselective synthesis of six 5,7-dimethylindolizidine isomers is described via an intramolecular cyclization that involves an allylsilyl nucleophilic group and an acyliminium ion. The first total synthesis of naturally occurring (-)-dendroprimine has been achieved in five steps.

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