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Convolvine, a naturally occurring alkaloid found in the roots and stems of the tropical plant Rauvolfia serpentina, belongs to a class of organic compounds with basic nitrogen atoms. It has demonstrated potential pharmaceutical applications, particularly in cardiovascular health and blood pressure management, due to its vasodilatory properties that improve blood flow and reduce strain on the heart.

537-30-4

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537-30-4 Usage

Uses

Used in Pharmaceutical Industry:
Convolvine is used as a vasodilator for its ability to widen blood vessels and enhance blood flow, which can help in reducing the strain on the heart and lowering blood pressure. This makes it a promising candidate for the treatment of cardiovascular diseases and hypertension.
Used in Cancer Research:
Convolvine is used as a potential inhibitor of certain cancer cell growth. While more research is required to fully understand its capabilities and mechanisms, its potential in this area highlights its versatility as a medicinal compound with possible therapeutic benefits in oncology.

Check Digit Verification of cas no

The CAS Registry Mumber 537-30-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,3 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 537-30:
(5*5)+(4*3)+(3*7)+(2*3)+(1*0)=64
64 % 10 = 4
So 537-30-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H21NO4/c1-19-14-6-3-10(7-15(14)20-2)16(18)21-13-8-11-4-5-12(9-13)17-11/h3,6-7,11-13,17H,4-5,8-9H2,1-2H3

537-30-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Veratric acid, 3.α.-nortropanyl ester

1.2 Other means of identification

Product number -
Other names Veratrumsaeure-nortropan-3endo-ylester

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:537-30-4 SDS

537-30-4Relevant academic research and scientific papers

Synthesis of N -(Hetero)arylconvolvine Derivatives through a Palladium-Catalyzed Buchwald-Hartwig Cross-Coupling

Alami, Mouad,Ghermani, Noureddine,Hassine, Manel,Jannet, Hichem Ben,Messaoudi, Samir

, p. 450 - 458 (2020/01/23)

The present study describes the isolation of convolvine from the roots of the Tunisian plant Convolvulus dorycnium L. and its synthesis through a four-step sequence starting from tropine. Then, an efficient synthesis of N -(het)aryltropanes derivatives by

CONVOLINE - A NEW ALKALOID FROM Convolvulus krauseanus

Aripova, S. F.,Sharova, E. G.,Abdullaev, U. A.,Yunusov, S. Yu.

, p. 712 - 714 (2007/10/02)

A new alkaloid has been isolated from the epigeal part of Convolvulus krauseanus Regel. et Schmalh., and its structure has been established as (+/-)-3-veratroyl-N-hydroxynortropane.

ALKALOIDS OF Convolvulus subhirsutus

Sharova, E. G.,Aripova, S. F.,Yunusov, S. Yu.

, p. 487 - 490 (2007/10/02)

The total alkaloids of the roots of Convolvulus subhirsutus collected in the period of vigorous growth close to the village of Dzhilga, Chimkent province, have been studied.From the phenolic fraction of the total alkaloids of this species of plant we have isolated phyllalbine and convolidine for the first time.From the nonphenolic fraction of the combined bases we isolated convolvine, which has been found previously, the new alkaloid confoline, and an unidentified base (III).On the basis of spectral characteristics and some spectral transformations it has been established that confoline has the structure of (+)-N-formylconvolvine.

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