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Octahydro-1,5-methanopentalene is a cyclic alkane with the molecular formula C6H12. It is a saturated hydrocarbon, meaning it contains only single bonds between carbon atoms. The compound features a five-membered ring with one additional carbon atom attached to two of the ring's carbons, forming a six-membered ring structure. This unique arrangement of carbon atoms results in a highly strained molecule due to the angle strain caused by the fusion of the two rings. Octahydro-1,5-methanopentalene is an interesting molecule in organic chemistry, as it provides insights into the effects of ring strain on molecular properties and reactivity.

1521-75-1

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1521-75-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1521-75-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,2 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1521-75:
(6*1)+(5*5)+(4*2)+(3*1)+(2*7)+(1*5)=61
61 % 10 = 1
So 1521-75-1 is a valid CAS Registry Number.

1521-75-1SDS

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 tricyclo[4.2.1.03.9]nonane

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 -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1521-75-1 SDS

1521-75-1Downstream Products

1521-75-1Relevant academic research and scientific papers

Hydrogenolysis of Small Cycloalkanes, XIII - Hydrogenation of Homucubane Derivatives

Osawa, Eiji,Schneider, Ingrid,Toyne, Kennet J.,Musso, Hans

, p. 2350 - 2361 (2007/10/02)

Two dihydro products 5a and 7a are formed by hydrogenation of homocubane (6a) with Pd-, Pt-, and Rh-catalysts.Only the unsymmetric 7a reacts further to give twistbrendane (8a).In addition, ca. 20percent brendane (11a) is obtained by hydrogenation of homocuneane (9a), which is formed from 6a by rearrangement on the catalyst.The yield of the symmetric dihydro product 5b is raised up to 40percent in the case of hydrogenation of the ethylene acetal 6b of the 9-ketone on Rh/Al2O3.With the ester 6d no 5d is obtained but 7d and 8d only.

ADDITION OF ORGANIC ACIDS TO cis-BICYCLONONA-3,7-DIENE. SYNTHESIS OF COMPOUNDS OF THE BREXANE AND BRENDANE SERIES

Arbuzov, V. A.,Gevorkyan, G. G.,Pekhk, T. I.,Bobyleva, N. A.,Belikova, N. A.

, p. 1114 - 1124 (2007/10/02)

The esters of cis-bicyclononenols, exo- and endo-brexan-5-ols, and exo-brendan-2-ol were obtained by the addition of formic, acetic, and trifluoroacetic acids to cis-bicyclonona-3,7-diene.The composition of the reaction products and its dependence on the reaction conditions were determined.A method is proposed for the separation of the bicyclic and tricyclic components.The mechanism of the transannular cyclization is discussed.

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