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Cyclohexene, 3,6-dibromo-, cis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

42086-54-4

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42086-54-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42086-54-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,0,8 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 42086-54:
(7*4)+(6*2)+(5*0)+(4*8)+(3*6)+(2*5)+(1*4)=104
104 % 10 = 4
So 42086-54-4 is a valid CAS Registry Number.

42086-54-4SDS

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 cis-3,6-dibromocyclohexene

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:42086-54-4 SDS

42086-54-4Upstream product

42086-54-4Relevant academic research and scientific papers

Desymmetrization of meso-Dibromocycloalkenes through Copper(I)-Catalyzed Asymmetric Allylic Substitution with Organolithium Reagents

Goh, Shermin S.,Guduguntla, Sureshbabu,Kikuchi, Takashi,Lutz, Martin,Otten, Edwin,Fujita, Makoto,Feringa, Ben L.

supporting information, p. 7052 - 7055 (2018/06/01)

The highly regio- and enantioselective (up to >99:1 dr, up to 99:1 er) desymmetrization of meso-1,4-dibromocycloalk-2-enes using asymmetric allylic substitution with organolithium reagents to afford enantioenriched bromocycloalkenes (ring size of 5 to 7)

Stereoselective halogenations of alkenes and alkynes in ionic liquids

Chiappe, Cinzia,Capraro, Dario,Conte, Valeria,Pieraccini, Daniela

, p. 1061 - 1063 (2007/10/03)

(matrix presented) Room-temperature ionic liquids, 1-butyl-3-methylimidazolium hexafluorophosphate, 1-butyl-3-methylimidazolium tetrafluoroborate, 1-butyl-3-methylimidazolium bromide, and 1-butyl-3-methylimidazolium chloride, are used as "green" recyclabl

Bromination of Cyclohexa-1,3-diene and (R,S)-Cyclohexa-3,5-diene-1,2-diol

Han, Xinghua,Khedekar, Rajashree N.,Masnovi, John,Baker, Ronald J.

, p. 5245 - 5250 (2007/10/03)

The configuration of 1,2,3,4-tetrabromocyclohexane (mp 90°C), 5a, has been established as 1,2t,3t,4c by an X-ray crystallographic determination. The structures of two of three dibromocyclohexenes (3a, 3b, and 3c) have been reassigned on the basis of NMR e

An Investigation of the Retro Diels-Alder Reaction as a Method for the Generation of Diatomic Sulfur

Gilchrist, Thomas L.,Wood, Jane E.

, p. 9 - 16 (2007/10/02)

The cyclic disulfides 2,3-dithiabicyclooct-5-ene 5, 1,4-dihydro-2,3-benzodithin 6 and hexahydro-5,8-epoxy-2,3-benzodithiin 7 have been prepared by oxidation of the corresponding dithiols.Each of these compounds has been subjected to vapour phase pyrolysis in order to determine whether a retro Diels-Alder reaction occurs, leading to the formation of diatomic sulfur (S2) and a diene.Compounds 5 and 7 both appeared to decompose in this way; in each case the expected diene was detected in the pyrolysate together with sulfur (S8).Attempts to intercept S2 and thus to obtain direct evidence for its formation were not successful.The benzodithiin 6 underwent an analogous loss of sulfur on vapour phase pyrolysis, but only as a minor reaction pathway, and this decomposition pathway was not detectable in solution pyrolyses.Solution pyrolysis of 6 in the presence of N-phenylmaleinimide gave N-phenyl-2,3-naphthalimide 21 in low yield. cis-Cyclopentene-3,5-dithiol 9 has also been prepared but no evidence could be obtained for the formation of disulfide 4 on oxidation.Reaction of the dithiol 9 with aldehydes and ketones in the presence of acids led to the formation of adducts (such as 12 and 13 from acetone) which were rapidly interconverted in acidic media.

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