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(3Z)-3-(hydroxymethylidene)octahydro-1,8-methanocyclopenta[c]pentalen-2(1H)-one is a cyclic ketone with a unique and rigid molecular framework, featuring a four-carbon ring fused to a six-carbon ring and a hydroxymethylidene group. (3Z)-3-(hydroxymethylidene)octahydro-1,8-methanocyclopenta[c]pentalen-2(1H)-one belongs to the methanocyclopenta[c]pentalene family and may exhibit potential reactivity and stability due to its cycloalkane structure.

82353-33-1

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82353-33-1 Usage

Uses

Used in Organic Synthesis:
(3Z)-3-(hydroxymethylidene)octahydro-1,8-methanocyclopenta[c]pentalen-2(1H)-one is used as a synthetic intermediate for the preparation of various organic compounds, taking advantage of its unique structure and potential reactivity.
Used in Pharmaceutical Industry:
(3Z)-3-(hydroxymethylidene)octahydro-1,8-methanocyclopenta[c]pentalen-2(1H)-one is used as a building block for the development of pharmaceuticals, given its potential to form novel drug candidates with unique properties and activities.
Used in Materials Science:
(3Z)-3-(hydroxymethylidene)octahydro-1,8-methanocyclopenta[c]pentalen-2(1H)-one is used as a component in the design and synthesis of new materials, such as polymers or composites, due to its rigid molecular framework and potential for molecular interactions.

Check Digit Verification of cas no

The CAS Registry Mumber 82353-33-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,3,5 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 82353-33:
(7*8)+(6*2)+(5*3)+(4*5)+(3*3)+(2*3)+(1*3)=121
121 % 10 = 1
So 82353-33-1 is a valid CAS Registry Number.

82353-33-1Downstream Products

82353-33-1Relevant academic research and scientific papers

SYNTHESIS OF FENESTRANE AND A FENESTRANE DERIVATIVE

Dauben, William G.,Walker, Daniel M.

, p. 711 - 714 (1982)

The synthesis of tetracyclo4,12.09,12>dodecan-6-one 12 via an intramolecular photocycloaddition, its reduction to the hydrocarbon 13 and its ring-contraction to tetracyclo-3,11.09,11>undecane derivative 16 is described.

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