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1-Oxaspiro[2.2]pentane, 2-methyl-2-phenyl- is a complex organic chemical compound with the molecular formula C12H14O. It is a spiro compound, which means it contains a spiro atom (in this case, oxygen) that is bonded to two other ring systems. The compound consists of a five-membered oxaspiro ring with a methyl group at the 2-position and a phenyl group also at the 2-position. This unique structure gives it specific chemical properties and potential applications in various fields, such as pharmaceuticals, agrochemicals, or materials science. Due to its complex structure, it is essential to handle 1-Oxaspiro[2.2]pentane, 2-methyl-2-phenyl- with care and follow proper safety guidelines during synthesis and usage.

75749-98-3

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75749-98-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75749-98-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,7,4 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 75749-98:
(7*7)+(6*5)+(5*7)+(4*4)+(3*9)+(2*9)+(1*8)=183
183 % 10 = 3
So 75749-98-3 is a valid CAS Registry Number.

75749-98-3Downstream Products

75749-98-3Relevant academic research and scientific papers

Catalytic and regioselective ring expansion of arylcyclobutanones with trimethylsilyldiazomethane. Ligand-dependent entry to β-ketosilane or enolsilane adducts

Dabrowski, Jennifer A.,Moebius, David C.,Wommack, Andrew J.,Kornahrens, Anne F.,Kingsbury, Jason S.

supporting information; experimental part, p. 3598 - 3601 (2010/11/04)

Divergent reactivity is uncovered in the homologation of arylcyclobutanones with trimethylsilyldiazomethane. With Sc(OTf)3 as catalyst, enolsilanes are obtained with a high preference for methylene migration. By contrast, Sc(hfac)3 g

EXPLORATORY STUDY ON α-METALLO SELENONES : Original Syntheses of Oxaspiropentanes.

Krief, A.,Dumont W.,Laboureur, J.L.

, p. 3265 - 3268 (2007/10/02)

Oxaspiropentanes have been obtained from α-metallocyclopropyl phenyl selenones and carbonyl compounds and on reaction of a base with β-hydroxyalkyl cyclopropyl selenones.The original reactivity of other β-hydroxyalkyl selenones is also disclosed.

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