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Methyl (5xi,6alpha)-6-bromo-12-methoxy-7-oxopodocarpa-8,11,13-trien-16-oate is a complex organic compound with the molecular formula C19H23BrO5. It is a derivative of podocarpic acid, a naturally occurring diterpenoid with potential anti-cancer properties. The compound features a 6-bromo substituent, a 12-methoxy group, and a 7-oxo functional group, which contribute to its unique chemical properties and potential biological activities. methyl (5xi,6alpha)-6-bromo-12-methoxy-7-oxopodocarpa-8,11,13-trien-16-oate is of interest in the field of natural product chemistry and may have applications in drug development, particularly in the area of cancer research.

1045-54-1

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1045-54-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1045-54-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,4 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1045-54:
(6*1)+(5*0)+(4*4)+(3*5)+(2*5)+(1*4)=51
51 % 10 = 1
So 1045-54-1 is a valid CAS Registry Number.

1045-54-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl (1S,4aS,10R)-10-bromo-6-methoxy-1,4a-dimethyl-9-oxo-3,4,10,10a-tetrahydro-2H-phenanthrene-1-carboxylate

1.2 Other means of identification

Product number -
Other names Podocarpa-8,11,13-trien-16-oic acid,6alpha-bromo-12-methoxy-7-oxo-,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:1045-54-1 SDS

1045-54-1Relevant academic research and scientific papers

Investigation of the antitumor activity of podocarpic acid derivatives

Parish,Miles

, p. 694 - 696 (1984)

As a class, octahydrophenanthrene lactones, podolactones, and related podocarpic acid derivatives have been reported to possess a wide variety of biological activities, including antileukemic activity, inhibition of plant cell growth, and hormonal and anti-inflammatory properties. In the present study, a series of synthetic intermediates derived from podocarpic acid have been prepared and evaluated with the respect to their ability to inhibit human epidermoid carcinoma of the nasopharynx in vitro. The significant cytotoxicity demonstrated by methyl 6α-bromo-7-oxo-O-methylpodocarpate (50% inhibition at 8.85 x 10-9 M) was markedly higher than that of the other derivatives examined. Further evaluation against L210 and P388 lymphoid leukemias in mice failed to demonstrate significant antitumor activity.

Reactions of η2-tetracarbonylmanganese complexes derived from podocarpic acid with electrophiles; functionalization of ring C

Cambie, Richard C.,Metzler, Michael R.,Rickard, Clifton E. F.,Rutledge, Peter S.,Woodgate, Paul D.

, p. 177 - 198 (2007/10/02)

Reaction of tetracarbonylmanganese(I) complexes derived from podocarpic acid (1) with electrophilic bromine or iodine in CCl4 leads to 14-halogenated derivatives inaccessible by direct halogenation.Similar reactions in protic solvents lead to the formation of γ-lactones in high yield.The structure of one of these was established unequivocally by X-ray crystallograohy.Attempted oxidation of the C-Mn bond with a number of reagents proved generally to be unsuccessful.

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