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ervayunine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

120202-64-4

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120202-64-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120202-64-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,2,0 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 120202-64:
(8*1)+(7*2)+(6*0)+(5*2)+(4*0)+(3*2)+(2*6)+(1*4)=54
54 % 10 = 4
So 120202-64-4 is a valid CAS Registry Number.
InChI:InChI=1/C19H24N2O/c1-2-19-9-7-16-14(13-5-3-4-6-15(13)20-16)8-10-21(12-19)11-17-18(19)22-17/h3-6,17-18,20H,2,7-12H2,1H3

120202-64-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Ervayunine

1.2 Other means of identification

Product number -
Other names -

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:120202-64-4 SDS

120202-64-4Downstream Products

120202-64-4Relevant academic research and scientific papers

TERPENOID INDOLE BIOTRANSFORMATION CAPACITY OF SUSPENSION CULTURES OF TABERNAEMONTANA DIVARICATA

Dagnino, Denise,Schripsema, Jan,Verpoorte, Robert

, p. 671 - 676 (1994)

Two cell lines of Tabernaemontana divaricata derived from the same suspension culture were compared with respect to their biotransformation capacity.One is high indole alkaloid-producing culture wich accumulated mainly O-acetylvallesamine.The other cell line biosynthesizes terpenoid indole alkaloids in much lower amounts.Both cell lines were cultured in medium containing either conopharyngine, coronaridine, vobasine or tabersonine.Chemical breakdown was followed in fresh and the used culture medium in the absence of cell culture.All the alkaloids investigated underwent chemical transformation.Most of the biotransformation products accumulated by the cultures have been reported to occur in intact plants.Since all the alkaloids added were transformed in the same way by both cultures, the two cell lines seem to have the same biotrasformation potential.

Synthesis of vinca alkaloids and related compounds. 100. Stereoselective oxidation reactions of compounds with the aspidospermane and quebrachamine ring system. First synthesis of some alkaloids containing the epoxy ring

Eles, Janos,Kalaus, Gyoergy,Greiner, Istvan,Kajtar-Peredy, Maria,Szabo, Pal,Keseru, Gyoergy Miklos,Szabo, Lajos,Szantay, Csaba

, p. 7255 - 7260 (2002)

The first syntheses of the alkaloids (-)-mehranine (3), (+)-voaphylline/conoflorine (4), (+)-Na-methylvoaphylline/hecubine (5), and (-)-lochnericine (2) were achieved by stereoselective epoxidation starting from (-)-tabersonine (1), through intermediates with the aspidospermane and quebrachamine skeleton.

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