Cabergolinic acid methyl ester Hydrobromide

Cabergolinic acid methyl ester Hydrobromide - Names and Identifiers

Name	6-(2-propenyl)-ergoline-8-carboxylic Acid Methyl Ester
Synonyms	Cabergoline Impurity 9 IACRGBGBDYCBKO-PUJMQQBBSA-N 6-Allyl-8β-carboxyergoline Methyl Ester Cabergolinic acid methyl ester Hydrobromide 6-(2-propenyl)-ergoline-8-carboxylic Acid Methyl Ester 6-(2-PROPENYL)-ERGOLINE-8-CARBOXYLIC ACID METHYL ESTER Ergoline-8-carboxylic acid, 6-(2-propen-1-yl)-, methyl ester, (8β)- Ergoline-8-carboxylic acid, 6-(2-propen-1-yl)-, Methyl ester, (8.beta.)- methyl (9R)-7-allyl-6,6a,8,9,10,10a-hexahydro-4H-indolo[4,3-fg]quinoline-9-carboxylate
CAS	72821-79-5

Cabergolinic acid methyl ester Hydrobromide - Physico-chemical Properties

Molecular Formula	C19H22N2O2
Molar Mass	310.4
Density	1.190±0.06 g/cm3(Predicted)
Boling Point	474.1±45.0 °C(Predicted)
pKa	17.52±0.40(Predicted)
Storage Condition	2-8℃

Cabergolinic acid methyl ester Hydrobromide - Risk and Safety

Hazard Class

IRRITANT

Cabergolinic acid methyl ester Hydrobromide - Introduction

Methyl 8β)-6-allylergole-8-carboxylate is an organic compound. The following is a description of its nature, use, formulation and safety information:

Properties: 8β)-6-allylergoline-8-carboxylic acid methyl ester is a solid, usually present as a white crystalline powder. It is almost insoluble in water at room temperature, but can be dissolved in organic solvents. The chemical structure of this compound contains lygic acid ester and allyl group.

use: 8β)-6-allyl ergoline -8-carboxylic acid methyl ester is a biologically active compound. It is used in the field of medicine as a precursor for the synthesis of derivatives of yergotic acid. This compound also has potential anti-inflammatory, antioxidant and antibacterial activities, and may therefore have applications in medical and health care products.

Preparation method: The preparation method of 8β)-6-allylergoline-8-carboxylic acid methyl ester involves a multi-step reaction. Lykeric acid needs to be obtained first, and then converted to 8β)-6-allyllykeric acid through a synthetic chemical reaction. Finally, 8β)-6-allylergoline-8-carboxylic acid methyl ester was prepared by esterification of lygic acid carboxyl group with methanol.

Safety information: Due to the lack of specific safety data, all potential hazards and safety information of this compound need to be further tested and studied. When handling and handling the compound, care should be taken to follow laboratory safety procedures, use appropriate personal protective equipment, and avoid direct contact with skin and inhalation of its dust. To ensure safety, always use the compound under the guidance of suitable facilities and professionals.

Last Update：2024-04-09 21:00:56