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39207-65-3

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39207-65-3 Usage

Uses

2-Isobutyrylcyclohexanone can be used as antitumor agents.

Check Digit Verification of cas no

The CAS Registry Mumber 39207-65-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,2,0 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 39207-65:
(7*3)+(6*9)+(5*2)+(4*0)+(3*7)+(2*6)+(1*5)=123
123 % 10 = 3
So 39207-65-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H16O2/c1-7(2)10(12)8-5-3-4-6-9(8)11/h7-8H,3-6H2,1-2H3

39207-65-3 Well-known Company Product Price

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  • Aldrich

  • (682675)  2-Isobutyrylcyclohexanone  96%

  • 39207-65-3

  • 682675-1G

  • 854.10CNY

  • Detail
  • Aldrich

  • (682675)  2-Isobutyrylcyclohexanone  96%

  • 39207-65-3

  • 682675-5G

  • 3,204.63CNY

  • Detail

39207-65-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Isobutyrylcyclohexanone

1.2 Other means of identification

Product number -
Other names 2-(2-methylpropanoyl)cyclohexan-1-one

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:39207-65-3 SDS

39207-65-3Relevant articles and documents

Method for preparing alkane carboxylic acid by increasing alkane carbon chains

-

Paragraph 0031; 0045; 0048, (2021/06/09)

The invention discloses a method for preparing alkane carboxylic acid by increasing alkane carbon chains. The method comprises the following steps: (1) carrying out Stork enamine alkylation on cyclopentanone or cyclohexanone and a secondary amine compound to generate a corresponding 1-position secondary amine substituted cyclopentene or cyclohexene crude product, namely Stork enamine; (2) carrying out electrophilic reagent reaction on the Stork enamine and acyl halide to form a 2-acyl cyclic ketone compound; and (3) carrying out ring opening on the 2-acyl cyclic ketone compound under the action of alkali to generate a carbonyl carboxylic acid compound, and carrying out a Wolff-Huang Minglong reduction reaction on the carbonyl carboxylic acid compound to obtain the corresponding alkane carboxylic acid. According to the method disclosed by the invention, cyclopentanone or cyclohexanone can be flexibly selected to meet the requirement of increasing different carbon numbers according to the required carbon number and different sources of target carburant alkane carboxylic acid or corresponding acyl halide. The method has the advantages of simple reaction process and no complex operation difficulty, and is suitable for industrial mass production.

Targeting Staphylococcus aureus quorum sensing with nonpeptidic small molecule inhibitors

Murray, Ewan J.,Crowley, Rebecca C.,Truman, Alex,Clarke, Simon R.,Cottam, James A.,Jadhav, Gopal P.,Steele, Victoria R.,O'Shea, Paul,Lindholm, Catharina,Cockayne, Alan,Chhabra, Siri Ram,Chan, Weng C.,Williams, Paul

supporting information, p. 2813 - 2819 (2014/04/17)

A series of 3-oxo-C12-HSL, tetramic acid, and tetronic acid analogues were synthesized to gain insights into the structural requirements for quorum sensing inhibition in Staphylococcus aureus. Compounds active against agr were noncompetitive inhibitors of the autoinducing peptide (AIP) activated AgrC receptor, by altering the activation efficacy of the cognate AIP-1. They appeared to act as negative allosteric modulators and are exemplified by 3-tetradecanoyltetronic acid 17, which reduced nasal cell colonization and arthritis in a murine infection model.

Amidine dications as superelectrophiles

Corr, Michael J.,Roydhouse, Mark D.,Gibson, Kirsty F.,Zhou, Sheng-Ze,Kennedy, Alan R.,Murphy, John A.

supporting information; experimental part, p. 17980 - 17985 (2010/04/01)

2-Dimethylalkylammonium pyridinium and 2-dimethylalkylammonium pyrimidinium ditriflate salts are very powerful methylating agents toward phosphorus (triphenylphosphine) and nitrogen (triethylamine) nucleophiles. In competition experiments with triethylamine as nucleophile, these N-methyl disalts are more reactive methylating agents than dimethyl sulfate. Reaction of the pyridinium dications with water as an oxygen nucleophile leads to attack at the 2-position of the heteroaromatic ring and displacement of an ammonium group; 2-hydroxypyridinium compounds are formed in the first instance, which are easily converted to 2-pyridones. Extending the scope of the reactions, a tricationic 2,6-bis(dimethylalkylammonium) pyridinium salt has also been prepared and characterized and its reactivity as a methylating agent assessed in comparison with that of the dications.

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