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1-Acetyl-2-methylcyclopentane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1601-00-9

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1601-00-9 Usage

Physical state

Colorless liquid

Odor

Sweet, fruity

Uses

a. Production of fragrances
b. Solvent in various industrial processes
c. Potential use as a fuel additive
d. Potential use in pharmaceutical applications

Toxicity

Low toxicity

Safety

Relatively safe for use in applications mentioned above

Further research

Needed to fully understand potential uses and any potential risks associated with its use

Check Digit Verification of cas no

The CAS Registry Mumber 1601-00-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,0 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1601-00:
(6*1)+(5*6)+(4*0)+(3*1)+(2*0)+(1*0)=39
39 % 10 = 9
So 1601-00-9 is a valid CAS Registry Number.

1601-00-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-acetyl-2-methylcyclopentane

1.2 Other means of identification

Product number -
Other names Ethanone, 1-(2-methylcyclopentyl)-

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:1601-00-9 SDS

1601-00-9Relevant academic research and scientific papers

TRANSFORMATIONS OF CYCLOALKANES UNDER THE ACTION OF ACYL HALIDES IN THE PRESENCE OF AlBr3.

Akhrem, I.S.,Orlinkov, A.V.,Mysov, E.I.,Vol'pin, M.E.

, p. 3891 - 3894 (1981)

Cycloalkanes have been found to react with acyl halides in the presence of AlBr3 ( mole ratio RCOX:AlBr3=1:2 ) under very mild conditions affording products of hydrocarbon oxidative coupling or/and hydrocarbon acylation.

Electrochemical Coupling of Biomass-Derived Acids: New C8 Platforms for Renewable Polymers and Fuels

Wu, Linglin,Mascal, Mark,Farmer, Thomas J.,Arnaud, Sacha Pérocheau,Wong Chang, Maria-Angelica

, p. 166 - 170 (2017/01/17)

Electrolysis of biomass-derived carbonyl compounds is an alternative to condensation chemistry for supplying products with chain length >C6for biofuels and renewable materials production. Kolbe coupling of biomass-derived levulinic acid is used to obtain 2,7-octanedione, a new platform molecule only two low process-intensity steps removed from raw biomass. Hydrogenation to 2,7-octanediol provides a chiral secondary diol largely unknown to polymer chemistry, whereas intramolecular aldol condensation followed by hydrogenation yields branched cycloalkanes suitable for use as high-octane, cellulosic gasoline. Analogous electrolysis of an itaconic acid-derived methylsuccinic monoester yields a chiral 2,5-dimethyladipic acid diester, another underutilized monomer owing to lack of availability.

COMPOUNDS USEFUL AS MODULATORS OF TRPM8

-

Paragraph 0601, (2016/03/29)

The present invention includes compounds useful as modulators of TRPM8, such as compounds of Formulae (Ia), (Ib) and (Ic), and the subgenus and species thereof; personal products containing those compounds; and the use of those compounds and the personal products, particularly the use of increasing or inducing chemesthetic sensations, such as cooling or cold sensations.

Cu-catalyzed asymmetric conjugate additions of alkylzinc reagents to acyclic aliphatic enones

Mizutani, Hirotake,Degrado, Sylvia J.,Hoveyda, Amir H.

, p. 779 - 781 (2007/10/03)

Cu-catalyzed enantioselective conjugate additions to acyclic aliphatic enones are reported. The resulting enolates may be functionalized intra- and intermolecularly, leading to the formation of an additional C-C bond. The utility of the present method is not limited to reactions involving Et2Zn; a variety of alkylzincs may be used. Moreover, many of the requisite substrates can be easily accessed through catalytic olefin cross metathesis. Copyright

Efficient Cu-catalyzed asymmetric conjugate additions of alkylzincs to trisubstituted cyclic enones

Degrado, Sylvia J.,Mizutani, Hirotake,Hoveyda, Amir H.

, p. 13362 - 13363 (2007/10/03)

The first examples of efficient catalytic asymmetric conjugate addition (ACA) of alkylzincs to trisubstituted cyclic enones is disclosed. These Cu-catalyzed reactions proceed efficiently with five- and seven-membered ring substrates to afford the desired products in ≥95% ee. Intermediate enolates can be trapped with alkyl halides to generate a quaternary stereogenic center. The requisite chiral ligand is prepared from commercially available materials and can be used in situ without further purification in the presence of commercial grade (CuOTf)2·PhMe. Copyright

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