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3-Methyl-4-penten-2-one, also known as isopropenyl acetone or mesityl oxide, is a colorless liquid organic compound with the chemical formula C6H10O. It is an unsaturated ketone, featuring a methyl group attached to the third carbon and a carbonyl group at the second carbon of a pentene chain. 3-Methyl-4-penten-2-one is widely used as a solvent, a reagent in organic synthesis, and a precursor in the production of various chemicals, including perfumes, pharmaceuticals, and flavorings. It is also known for its ability to dissolve a variety of substances and its use in the synthesis of resins and plastics. 3-Methyl-4-penten-2-one is produced industrially through the dehydration of 3-methyl-3-pentanol or by the oxidation of 3-methyl-2-buten-1-ol. It is characterized by a pungent, peppery odor and is considered a hazardous substance due to its irritant and flammable properties.

758-87-2

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758-87-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 758-87-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,5 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 758-87:
(5*7)+(4*5)+(3*8)+(2*8)+(1*7)=102
102 % 10 = 2
So 758-87-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O/c1-4-5(2)6(3)7/h4-5H,1H2,2-3H3

758-87-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methylpent-4-en-2-one

1.2 Other means of identification

Product number -
Other names 4-Penten-2-on3,3-methyl

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:758-87-2 SDS

758-87-2Downstream Products

758-87-2Relevant academic research and scientific papers

ALLYLCHLOROTINS AS ALLYLATING AGENTS OF ACYL CHLORIDES

Gambaro, Alessandro,Peruzzo, Valerio,Marton, Daniele

, p. 291 - 296 (1983)

Allylchlorotins of the type R(3-n)AllSnCln (R = alkyl or All; All = CH2=CHCH2 or cis/trans-CH3CH=CHCH2, n = 1-3) undergo uncatalyzed coupling with acyl chlorides under mild conditions.This reaction as well as the corresponding addition reaction to ketones are much faster when Cl is replaced by NCS group in the organotin derivative.

PROCESS FOR PREPARING PLATINUM ORGANOSILOXANE COMPLEXES USING AN ENONE ADDITIVE

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Paragraph 0023-0024, (2019/02/06)

A platinum organosiloxane complex is prepared by a process including combining A) a platinous halide; B) a ketone; C) an enone additive distinct from any other starting materials or rearrangement products thereof; and D) a polyorganosiloxane having, per molecule, 2 to 4 silicon bonded terminally unsaturated hydrocarbon groups having from 2 to 6 carbon. The platinum organosiloxane complex prepared by the process is useful as a hydrosilylation catalyst.

Photochemical Deconjugation of α,β-Unsaturated Ketones

Eng, Stephen L.,Ricard, Roland,Wan, Calvin S. K.,Weedon, Alan C.

, p. 236 - 238 (2007/10/02)

It is shown that 'photochemically inert' α,β-unsaturated ketones can undergo synthetically useful u.v.light induced deconjugation via photoenolization in the presence of a mild base, and the mechanism of this reaction has been examined by measurement of the relative quantum yield of deconjugation as a function of base and solvent; the results indicate two competing mechanisms for the reketonization of the intermediate dienols, one involving a thermal 1,5-sigmatropic hydrogen shift, and the other base-catalysed proton transfer.

REACTIONS OF TITANOCENE ALLYLS

Klei, E.,Teuben, J.H.,De Liefde Meijer, H.J.,Kwak, E.J.,Bruins, A.P.

, p. 327 - 339 (2007/10/02)

Cp2Tiη3-allyl and Cp2Tiη3-1-methylallyl react with carbon dioxide, phenylisocyanate, benzalaniline, acetone and acetonitrile to give insertion products which are formed via allyl migration.Normal insertion is observed with 2,6-xylylisocyanide.C

Titanium-promoted Allyl Transfer to Carbon Monoxide and Other Unsaturated Molecules

Klei, Bert,Teuben, Jan H.,Meijer, Henk J. de Liefde

, p. 342 - 344 (2007/10/02)

Carbonylation of Cp2Ti-(?-allyl) yields Cp2Ti(CO)2 and triallylmethanol; reactions of Cp2Ti-(?-allyl) and Cp2Ti-(?-1-methylallyl) with other ligands proceed via insertion or allyl-elimination pathways.

IMPROVED SYNTHESIS OF β,γ-UNSATURATED KETONES BY THE REACTION OF ALLYLIC ZINC BROMIDES WITH NITRILES.

Rousseau, G.,Conia, J. M.

, p. 649 - 652 (2007/10/02)

The reaction of allylic bromides with nitriles in the presence of Zn-Ag couple leads, after hydrolysis, to β,γ-unsaturated ketones in high yield.

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