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22223-16-1 Usage

Description

Russian workers have recently given the ketonic structure for this alkaloid, rather than the original epoxy structure.

References

Rakhimov et al., Khim. Prir. Soedin., 6, 226 (1970)

Check Digit Verification of cas no

The CAS Registry Mumber 22223-16-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,2,2 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 22223-16:
(7*2)+(6*2)+(5*2)+(4*2)+(3*3)+(2*1)+(1*6)=61
61 % 10 = 1
So 22223-16-1 is a valid CAS Registry Number.

22223-16-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name	(all-ξ)-6,7-epoxy-16-methoxy-2,3-didehydro-aspidospermidine-3-carboxylic acid methyl ester

1.2 Other means of identification

Product number	-
Other names	Lochnerinin

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:22223-16-1 SDS

22223-16-1Upstream product

29479-00-3 (-)-tabersonine hydrochloride

22223-16-1Downstream Products

22223-16-1Relevant articles and documents

Biotransformation of tabersonine in cell suspension cultures of Catharanthus roseus.

Furuya,Sakamoto,Iida,Asada,Yoshikawa,Sakai,Aimi

, p. 3065 - 3068 (2007/10/02)

To investigate the reactions involved in the biosynthesis of vindoline from tabersonine, the bioconversion products formed when the latter compound was fed to cell suspension cultures of Catharanthus roseus were isolated and characterized. Two biotransformation products of tabersonine were isolated and shown to be lochnericine, which is formed by epoxidation of tabersonine at positions 14, 15, and lochnerinine, the 11-methoxylation product of lochnericine. The bioconversion ratio of the main biotransformation product, lochnericine, reached a value of 80.6% within three days.

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CAS

22223-16-1