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1-Oxaspiro[4.5]decan-2-one, 4-methylene- is a complex organic chemical compound with the molecular formula C10H16O2. It is a cyclic ketone with a spiro structure, consisting of a seven-membered ring fused to a five-membered ring, and a methylene group (CH2) at the 4-position. 1-Oxaspiro[4.5]decan-2-one, 4-methylene- is characterized by its unique molecular structure, which contributes to its specific chemical properties and potential applications in various fields, such as pharmaceuticals, agrochemicals, or materials science. Due to its complex structure, it may require specialized synthesis methods and is typically of interest to researchers and chemists working in the field of organic synthesis.

93423-70-2

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93423-70-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93423-70-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,4,2 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 93423-70:
(7*9)+(6*3)+(5*4)+(4*2)+(3*3)+(2*7)+(1*0)=132
132 % 10 = 2
So 93423-70-2 is a valid CAS Registry Number.

93423-70-2Downstream Products

93423-70-2Relevant academic research and scientific papers

Samarium (II) iodide-induced intermolecular coupling of a,b-unsaturated esters with ketones: Reactions of methyl propiolate and ethyl buta-2,3-dienoate with cyclohexanone and its application to synthesis of a terpene carboxylic acid

Sono, Masakazu,Doi, Natsuki,Yoshino, Eri,Onishi, Sachiko,Fujii, Daiki,Tori, Motoo

supporting information, p. 1947 - 1950 (2013/04/10)

The reactions of methyl propiolate and ethyl buta-2,3-dienoate with cyclohexanone induced by SmI2 occurred either at a- or b-position to yield different products depending on with or without a proton source. The synthesis of terpenic acid was demonstrated using this reaction.

Unsaturated spiro-γ-lactone formation by the dissociative reduction of bromoacetates

Kolt,Griller,Wayner

, p. 7539 - 7540 (2007/10/02)

Unsaturated spiro-γ-butyrolactones can be prepared in good yields from bromoacetate precursors by a simple route that requires only 2-propanol as solvent and free radical initiation.

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