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928-68-7

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  • 98% 6-Methyl-2-heptanone CAS:928-68-7 CAS NO.928-68-7

    Cas No: 928-68-7

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928-68-7 Usage

Uses

6-Methyl-2-heptanone is used in the synthesis of antifungal crassinervic acid analogs. Also used in the synthesis of BACE-1 inhibitors in the treatment of Alzheimer’s disease.

Synthesis Reference(s)

Tetrahedron, 49, p. 8169, 1993 DOI: 10.1016/S0040-4020(01)88036-4

Check Digit Verification of cas no

The CAS Registry Mumber 928-68-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,2 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 928-68:
(5*9)+(4*2)+(3*8)+(2*6)+(1*8)=97
97 % 10 = 7
So 928-68-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O/c1-7(2)5-4-6-8(3)9/h7H,4-6H2,1-3H3

928-68-7SDS

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 6-Methyl-2-heptanone

1.2 Other means of identification

Product number -
Other names 6-methylheptan-2-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:928-68-7 SDS

928-68-7Relevant articles and documents

Tuning nano-nickel selectivity with tin in flow hydrogenation of 6-methyl-5-hepten-2-one by surface organometallic chemistry modification

Zienkiewicz-Machnik, Ma?gorzata,Goszewska, Ilona,?r?bowata, Anna,Kubas, Adam,Giziński, Damian,S?owik, Grzegorz,Matus, Krzysztof,Lisovytskiy, Dmytro,Pisarek, Marcin,Sá, Jacinto

, p. 38 - 44 (2018)

Chemoselective flow hydrogenation of 6-methyl-5-hepten-2-one was performed over nano-nickel catalysts. The parent catalyst composed solely of nickel nanoparticles grafted on the polymeric resin exhibited high activity and selectivity towards C[dbnd]C bond saturation but its modification with small quantities of tin significantly increased its ability to perform C[dbnd]O bond hydrogenation. The post-synthetic modification of the parent catalyst was achieved by surface organometallic chemistry approach and performed in the same flow micro-reactor, which was used for the catalytic studies, providing a methodology for online modification of parent catalysts.

Chemoselective Hydrogenation of Olefins Using a Nanostructured Nickel Catalyst

Klarner, Mara,Bieger, Sandra,Drechsler, Markus,Kempe, Rhett

supporting information, p. 2157 - 2161 (2021/05/21)

The selective hydrogenation of functionalized olefins is of great importance in the chemical and pharmaceutical industry. Here, we report on a nanostructured nickel catalyst that enables the selective hydrogenation of purely aliphatic and functionalized olefins under mild conditions. The earth-abundant metal catalyst allows the selective hydrogenation of sterically protected olefins and further tolerates functional groups such as carbonyls, esters, ethers and nitriles. The characterization of our catalyst revealed the formation of surface oxidized metallic nickel nanoparticles stabilized by a N-doped carbon layer on the active carbon support.

Tuning Nano-Nickel Catalyst Hydrogenation Aptitude by On-the-Fly Zirconium Doping

Zienkiewicz-Machnik, Ma?gorzata,Goszewska, Ilona,Giziński, Damian,?r?bowata, Anna,Kuzmowicz, Katarzyna,Kubas, Adam,Matus, Krzysztof,Lisovytskiy, Dmytro,Pisarek, Marcin,Jacinto

, p. 3132 - 3138 (2020/05/06)

The effect of nano-Ni catalyst post-synthetic Zr-modification on hydrogenation reaction of 6-methyl-5-hepten-2-one was investigated in a fixed bed continuous-flow micro-reactor to produce fine chemicals. The catalytic performance revealed that Zr-doping achieved by surface organometallic chemistry approach modifies the natural aptitude of nickel to hydrogenate C=C bond, since the addition of small quantities of zirconium significantly increased the amount of unsaturated and saturated alcohols formed in 6-methyl-5-hepten-2-one hydrogenation. Quantum chemical calculations revealed a stronger interaction between Zr←O=C that promotes the formation of C=C semihydrogenation product and enhances the probability of complete hydrogenation. The on-the-fly strategy presented herein enables for rapid optimization and understanding of catalytic processes.

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