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Exo-9-methoxybicyclo<6.1.0>nonane is a complex organic compound with the molecular formula C10H18O. It is a derivative of bicyclo[6.1.0]nonane, a bicyclic hydrocarbon, with a methoxy group (-OCH3) attached to the exo position of the molecule. The exo position refers to the side of the molecule that is not involved in the ring fusion, making the methoxy group more accessible and less sterically hindered. exo-9-methoxybicyclo<6.1.0>nonane is of interest in organic chemistry due to its unique structure and potential applications in the synthesis of various pharmaceuticals and other chemical products. It is characterized by its cyclic nature and the presence of a methoxy group, which can influence its reactivity and physical properties.

2988-71-8

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2988-71-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2988-71-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,8 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2988-71:
(6*2)+(5*9)+(4*8)+(3*8)+(2*7)+(1*1)=128
128 % 10 = 8
So 2988-71-8 is a valid CAS Registry Number.

2988-71-8Downstream Products

2988-71-8Relevant academic research and scientific papers

Deamination Reactions, 37. Decomposition of Bicyclononane- and Bicyclonon-2-ene-9-diazonium Ions

Kirmse, Wolfgang,Hellwig, Georg

, p. 2744 - 2754 (2007/10/02)

Bicyclononane-exo-9-diazonium ions (9) have been generated from the corresponding nitrosourea (8) and base.In weakly alkaline solution (E)-3-methoxycyclononene (11) was formed by disrotatory ring opening of (9).In the presence of sodium methoxide 1,2-cyclononadiene (13) and exo-9-methoxybicyclononane (15) were additional products, presumably arising via carbene 12.Bicyclonon-2-ene-exo-9-diazonium ions (21) decomposed without participation of the double bond to give the (Z,E)-methoxycyclononadienes 22 and 23.The 21-derived carbene 29 afforded the bicyclic ether 30 and the elusive 1,2,4-cyclononatriene (32).In contrast to its lower homologs, 29 did not undergo a carbene-carbene rearrangement (29 -> 31).

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