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Bicyclo[5.1.0]octane is a cyclic hydrocarbon compound with a unique molecular structure, consisting of two carbon rings fused together in a non-adjacent manner. It has the molecular formula C8H14 and is characterized by a bicyclic structure with one five-membered ring and one three-membered ring. The compound is known for its high thermal stability and resistance to chemical reactions, making it a potential candidate for various industrial applications, such as in the synthesis of pharmaceuticals and other organic compounds. Bicyclo[5.1.0]octane is also of interest to chemists due to its strained ring system, which can lead to interesting reactivity patterns and potential applications in the development of new materials.

286-43-1

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286-43-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 286-43-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,8 and 6 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 286-43:
(5*2)+(4*8)+(3*6)+(2*4)+(1*3)=71
71 % 10 = 1
So 286-43-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H14/c1-2-4-7-6-8(7)5-3-1/h7-8H,1-6H2/t7-,8+

286-43-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name bicyclo[5,1,0]octane

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
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More Details:286-43-1 SDS

286-43-1Upstream product

286-43-1Downstream Products

286-43-1Relevant academic research and scientific papers

Carbenes in Constrained Systems, 3. Solid-State Photolysis of Cycloheptane- and Cyclooctanespirodiazirine within Cyclodextrins and Zeolites

Kupfer, Rene,Brinker, Udo H.

, p. 1721 - 1726 (2007/10/03)

Inclusion complexes of cycloheptanespirodiazirine (1) and cyclooctanespirodiazirine (8) in α-, β-, and γ-cyclodextrin, and faujasite type zeolites (NaX and NaY), have been prepared.The guest-host complexes (1- and 8CD and 1- and 8zeolite) were irradiated with UV light in the solid state and the reaction products were separated from the host and analyzed.Product ratios from photolysis of complexes were compared with those obtained from pure compounds and in solution.Cycloheptanespirodiazirine (1) gives cycloheptene (2), bicycloheptane (3), and methylenecyclohexane (4).Photolysis products from cyclooctanespirodiazirine (8) are cyclooctene (9), bicyclooctane (10), and bicyclooctane (11). 10 results from a 1,5-C-H insertion reaction of the carbene derived from 8.As the cavity size of the cyclodextrins becomes larger, the formation of 10 seems to increase.In β-cyclodextrin and in non-polar solvents substantial amounts of azine were found.In addition to hydrocarbons, photolyses in zeolites afforded alcohols and small amounts of the corresponding ketones. - Keywords: Diazirines / Zeolites / Cyclodextrins / Photochemistry / Carbenes

Radiolysis of Cyclooctane with γ-Rays and Helium Ions

Wojnarovits, Laszlo,LaVerne, Jay A.

, p. 8014 - 8018 (2007/10/02)

Iodine scavenging techniques have been used to examine the role of the cyclooctyl radical in the radiolysis of cyclooctane with γ-rays and with 5-20-MeV helium ions.In γ-radiolysis about 70percent of the total yield of 6.6 cyclooctyl radicals/100 eV are scavenged with E-4 M iodine, which agrees well with other studies on cycloalkanes that show most of the radicals produced in these systems react in the bulk medium at times longer than 1 μs.However, it is found that 2.5 radicals/100 eV (38percent) are produced by H atom precursors as copmpared to a value of 1.5 cyclohexyl radicals/100 eV (25percent) in cyclohexane.With 10-MeV helium ions (average LET of 106 eV/nm), only 8percent of the cyclooctyl radicals survive longer than a few microseconds due to the increased initial radical concentration in the helium ion track.The yield of the cross-bridged product bicyclooctane (pentalane) was found to be independent of iodine concentration up to 0.03 M with both types of radiation.However, the pentalane yield found with 10-MeV helium ions was only one-third of that found in γ-radiolysis.The most likely reason for this result is the decreased yield of singlet-state formation due to the enhanced probability of cross combination reactions of electron-cation pairs in the high-density region of the helium ion track.

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