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Indolo[2,3-a]quinolizine,1-ethyl-2,3,4,6,7,12-hexahydro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

40163-47-1

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40163-47-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40163-47-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,1,6 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 40163-47:
(7*4)+(6*0)+(5*1)+(4*6)+(3*3)+(2*4)+(1*7)=81
81 % 10 = 1
So 40163-47-1 is a valid CAS Registry Number.

40163-47-1SDS

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 1-ethyl-2,3,4,6,7,12-hexahydro-indolo[2,3-a]quinolizine

1.2 Other means of identification

Product number -
Other names 1-Ethyl-2,3,4,6,7,12-hexahydro-indolo[2,3-a]quinolizine

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:40163-47-1 SDS

40163-47-1Relevant academic research and scientific papers

Efficient Synthesis of 1-Ethyl-2,3,4,6,7,12-hexahydroindoloquinolizine: a Key Precursor to Eburnane Alkaloids

Danieli, Bruno,Lesma, Giordano,Palmisano, Giovanni

, p. 109 (1980)

The title compond has been conveniently synthesized from the imine (3) by cyclisation with acrylic acid followed by reduction.

EASY PREPARATION OF INDOLOQUINOLIZIDINE ENAMINES

Lounasmaa, Mauri,Karvinen, Esko

, p. 489 - 497 (2007/10/02)

A new and efficient synthesis of indoloquinolizidine enamines, including the highly valuable Wenkert's enamine (9a), is described.The behaviour of enamines (9a) and (9b) under reductive conditions was investigated.

NOVEL APPLICATIONS OF THE MODIFIED POLONOVSKI REACTION - IX A NEW ROUTE TO WENKERT'S ENAMINE

Lounasmaa, Mauri,Karvinen, Esko,Koskinen, Ari,Jokela, Reija

, p. 2135 - 2146 (2007/10/02)

A practical synthetic entry to Wenkert's enamine 1 employing the modified Polonovski reaction is described.Complete 13 C NMR spectral data of 1 is presented.Conformational analysis of the intermediate 1-hydroxy- and 1-ethyl-1-hydroxy-indoloquinolizidines

Synthesis of vinca alkaloids and related compounds, XV. A new synthetic route to (+)-vincaminic and (+)-apovincaminic esters

Szabo,Kalaus,Szantay

, p. 629 - 638 (2007/10/02)

Esters of types 7 and 8, possessing excellent vasodilating effects, have been prepared. A method has been found for the resolution of methyl ester 7c. A new method is described for the preparation of the lactam (+)-10 and its conversion to the oxime (+)-11, from which (+)-vincamine (1a) and the (+)-apovincaminic esters 2a,b were synthesized.

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