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Spiro[2.3]hexane is a cyclic alkane with a unique structure, consisting of two six-membered carbon rings connected at a single carbon atom, forming a spiro junction. This organic compound is characterized by its molecular formula C6H10 and has a highly strained and rigid structure due to the presence of two fused cyclohexane rings. The molecule exhibits interesting chemical properties and has been studied for its potential applications in various fields, including materials science and pharmaceuticals. However, it is important to note that spiro[2.3]hexane is a highly reactive and unstable compound, which can pose challenges in its synthesis and handling.

157-45-9

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157-45-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 157-45-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,5 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 157-45:
(5*1)+(4*5)+(3*7)+(2*4)+(1*5)=59
59 % 10 = 9
So 157-45-9 is a valid CAS Registry Number.

157-45-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name spiro[2.3]hexane

1.2 Other means of identification

Product number -
Other names Spirohexane

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:157-45-9 SDS

157-45-9Relevant academic research and scientific papers

DER EINFLUSS VON WECHSELWIRKUNGEN DURCH DEN RAUM UND UEBER BINDUNGEN AUF DIE WALSH-ORBITALE VON SPIROCYCLOPROPYLVERBINDUNGEN

Hemmersbach, P.,Klessinger, M.

, p. 1337 - 1343 (1980)

The PE spectra of spiro- and dispirocyclopropyl derivatives of cyclobutane are investigated, and an assignment of the PE bands based on MINDO/3- and 4-31G calculations is proposed.The influence of the ?CH2 orbitals of the cyclobutane ring is discussed by means of a LCBO model: in the case of the 1,3-derivative through-bond interactions cause an inversion of the natural order of the orbitals, whereas through-space interactions reduce the conjugative splitting of the Walsh orbitals in the 1,2-derivative.The proposed model naturally explains also the various splittings of the Walsh orbitals in rotanes.

The non-reaction of methylene with the carbon-carbon bond

Wu, Guo-Xian,Maitland Jr., Jones,Doering, William von E.,Knox, Lawrence H.

, p. 9913 - 9920 (2007/10/03)

Methylene has been shown not to react with the carbon-carbon bonds of spiropentane and spiro[3.3]heptane.

REACTIONS OF DIAZOALKANES WITH UNSATURATED COMPOUNDS. 6. CATALYTIC CYCLOPROPANATION OF UNSATURATED HYDROCARBONS AND THEIR DERIVATIVES WITH DIAZOMETHANE

Dzhemilev, U. M.,Dokichev, V. A.,Sultanov, S. Z.,Khusnutdinov, R. I.,Tomilov, Yu. V.,et al.

, p. 1707 - 1714 (2007/10/02)

A systematic study has been conducted of the catalytic reaction of diazomethane with cyclic and polycyclic unsaturated hydrocarbons, conjugated dienes, as well as with a series of functionalized unsaturated conpounds.The feasibility of using transition metal, nontransition metal, and rare earth metal compounds of, for example, Co, Ni, Zr, Rh, and Dy, has been demonstrated for the first time.It has also been established that Pd(acac)2 has very high activity as a catalyst for the cyclopropanation of terminal and endocyclic double bonds by diazomethane, and that its activity is reduced upon the introduction of n-donor ligands or in the presence of strong polar solvents.

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