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3a,4,7,7a-tetrahydro-1H-4,7-methanoinden-1-one is a complex organic compound belonging to the class of indenes, which are derivatives of the parent compound indene. This specific compound is characterized by a unique molecular structure, featuring a saturated four-membered ring (tetrahydro) fused to a benzene ring, with a carbonyl group (C=O) at the 1-position and a methyl group (CH3) at the 7-position. The compound's molecular formula is C11H12O, and it exhibits a molecular weight of 160.21 g/mol. Due to its complex structure, 3a,4,7,7a-tetrahydro-1H-4,7-methanoinden-1-one has potential applications in various fields, such as pharmaceuticals, agrochemicals, and materials science, where it can be used as a building block for the synthesis of more complex molecules or as a precursor in chemical reactions.

5530-96-1

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5530-96-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5530-96-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,3 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5530-96:
(6*5)+(5*5)+(4*3)+(3*0)+(2*9)+(1*6)=91
91 % 10 = 1
So 5530-96-1 is a valid CAS Registry Number.

5530-96-1Upstream product

5530-96-1Relevant academic research and scientific papers

Regioselective Oxidation of Carbon-Carbon Double Bond of endo-Dicyclopentadiene

Pandey, Paras N.,Purkayastha, Makhan L.

, p. 717 - 719 (2007/10/02)

endo-9-Oxatetracyclo2.6.08.10>undec-3-ene (2) has been selectively prepared by the oxidation of endo-dicyclopentadiene (1) with chromium trioxide in acetic acid.On the other hand oxidation of 1 by pyridinium chlorochromate furnishes a 1 : 1 mixture of α-chloroketones (3 and 4) in high yield.A plausible mechanism is advanced to explain the formation of 3 and 4.

Dicyclopentadiene Oxidation I. Uncatalyzed Liquid-Phase Oxidation of Dicyclopentadiene

Schnurpfeil, D.

, p. 481 - 488 (2007/10/02)

Dicyclopentadiene is oxidized by molecular oxygen to a mixture of the monoepoxides 2 and 3.The identification of the epoxides 2, 3 and 4 was executed with authentic samples prepared by epoxidation with peracetic acid or with tert-butylhydroperoxide in the presence of MoO2(acac)2.The main product is the substituted norbornene oxide 2.Allylic oxidation is also observed.Remarkable amounts of hydroperoxides can be determined iodometrically.The formation of allylic oxidation products 7, 8, 9 and 10 was proved by GC-MS-analysis.It is shown that in the uncatalyzed liquid phase oxidation of dicyclopentadiene no more than 50 percent of epoxides are formed.The bisepoxide 4 was found in small amounts only at higher conversions of the dicyclopentadiene.

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