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Methyl O-methyl-Δ5,6-7-ketopodocarpate is a complex organic compound derived from podocarpic acid, a naturally occurring diterpenoid found in plants. This specific derivative features a methyl group attached to the oxygen atom of the podocarpic acid structure, as well as a double bond between carbons 5 and 6, and a ketone group at the 7 position. The compound is of interest in chemical research due to its potential biological activities and synthetic applications. It is often studied for its anti-inflammatory, anticancer, and antimicrobial properties, making it a candidate for pharmaceutical development. The synthesis and modification of such compounds can lead to the discovery of new drugs or agrochemicals.

1865-97-0

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1865-97-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1865-97-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,6 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1865-97:
(6*1)+(5*8)+(4*6)+(3*5)+(2*9)+(1*7)=110
110 % 10 = 0
So 1865-97-0 is a valid CAS Registry Number.

1865-97-0Relevant academic research and scientific papers

Reactions of podocarpic acid derivatives with thallium(III) nitrate

Miles,Lho,Chittawong,Payne

, p. 4034 - 4036 (2007/10/02)

The reaction of methyl O-methyl-7-ketopodocarpate (3) with thallium(III) nitrate in acetic acid was performed in attempt to synthesize compound 4, an intermediate in the total synthesis of the plant growth hormone gibberellic acid. The reaction unexpectedly resulted in new methodology for the one-step formation of methyl O-methyl-Δ5,6-7-ketopodocarpate from the keto ester 3. Four model compounds, having similar skeletons to the keto ester 3, were reacted with TTN under the same conditions to establish a general method for the formation of α,β-unsaturated ketones. These models yielded either the α-nitrato ketone and/or the decomposition product benzoic acid. Reaction of the hindered tricyclic ketone 11 with TTN yielded the expected α,β-unsaturated ketone 12. Thus this methodology is selective for hindered tricyclic ketone systems.

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