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50298-88-9

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50298-88-9 Usage

Uses

17,18-Dehydroapovincamine is an impurity of Vincamine (V314030), a nootropic agent to combat the effects of aging, or in conjunction with other nootropics (such as piracetam) for a variety of purposes. Vincamine is a peripheral vasodilator that increases blood flow to the brain.

Check Digit Verification of cas no

The CAS Registry Mumber 50298-88-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,2,9 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 50298-88:
(7*5)+(6*0)+(5*2)+(4*9)+(3*8)+(2*8)+(1*8)=129
129 % 10 = 9
So 50298-88-9 is a valid CAS Registry Number.

50298-88-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (+)-17,19-didehydroapovincamine

1.2 Other means of identification

Product number -
Other names 17,18-didehydro-eburnamenine-14-carboxylic acid methyl ester

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:50298-88-9 SDS

50298-88-9Upstream product

50298-88-9Downstream Products

50298-88-9Relevant articles and documents

Synthesis of new eburnamine-type alkaloid via direct hydroalkoxylation

Liu, Xiong,Yang, Dong-Liang,Liu, Jia-Jia,Zhou, Jing,Zhao, Nana

, p. 816 - 822 (2014)

This study concerns the preparation of a new eburnamine-type alkaloid, methyl (3α,14β,15β,16α)-17,18-didehydro-14,15- dihydroeburnamine-15-methoxy-14-carboxylate (VIII). This alkaloid was prepared from (+)-17,18-dehydroapovincamine (V) using Lewis acid and/or ion exchange resin as catalyst. The hydroalkoxylation reaction of V with methanol was investigated in terms of catalyst, solvent, temperature, and time of reaction. A one-pot method for synthetising this alkaloid was established. The optimal conditions for the reaction are discussed.

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