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4,4,5,5-Tetramethyl-2,7-octanedione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17663-27-3

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17663-27-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17663-27-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,6 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17663-27:
(7*1)+(6*7)+(5*6)+(4*6)+(3*3)+(2*2)+(1*7)=123
123 % 10 = 3
So 17663-27-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H22O2/c1-9(13)7-11(3,4)12(5,6)8-10(2)14/h7-8H2,1-6H3

17663-27-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4,5,5-tetramethyloctane-2,7-dione

1.2 Other means of identification

Product number -
Other names 4,4,5,5-TETRAMETHYL-2,7-OCTANEDIONE

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:17663-27-3 SDS

17663-27-3Downstream Products

17663-27-3Relevant academic research and scientific papers

HYDRODIMERIZATION OF UNSATURATED ALCOHOLS, ESTERS, NITRILES, KETONES, AMINES, SILANES, EPOXIDES AND FLUOROCARBONS BY MERCURY-PHOTOSENSITIZATION

Muedas, Cesar A.,Ferguson, Richard R.,Crabtree, Robert H.

, p. 3389 - 3392 (1989)

Substituted alkenes are efficiently hydrodimerized on a preparative scale in an H2 atmosphere by Hg(vapor) and 254 nm light.

Hydrogen Atoms as Convenient Synthetic Reagents: Mercury-Photosensitized Dimerization of Functionalized Organic Compounds in the Presence of H2

Muedas, Cesar A.,Ferguson, Richard R.,Brown, Stephen H.,Crabtree, Robert H.

, p. 2233 - 2242 (2007/10/02)

Hydrogen atoms are generated by mercury photosensitization in an unexceptional apparatus that makes them readily available for organic chemistry on a preparatively useful scale at 1 atm of pressure and temperatures from 0-150 °C. The H atoms add to CH2=CH-CH2X to give the intermediate radical CH3-(?CH)-CH2X, which dimerizes to give CH3CH(CH2X)-CH(CH2X)CH3. The saturated substrates CH3CH2CH2X undergo H abstraction to give CH3CH2(?CH)X as intermediates and CH3CH2CH(X)-CH(X)CH2CH3 as final products. The reaction shows a tolerance for different functional groups, X, which may be an alkyl or fluoroalkyl chain or contain vinyl, epoxy, ester, ketone, nitrile, and silyl groups. Radical disproportionation products are also formed but are easily separated. H atoms attack the weakest C-H bonds of the substrates with high selectivity. In our earliest direct mercury photosensitization, Hg* often failed to attack the substrate C-H bonds to give dimers; the presence of H2 strongly suppresses direct Hg* chemistry. H atoms are not sensitive to steric or polar effects Radical fragmentation is avoided by using "high" pressures (1 atm). Intramolecular radical additions to C=C bonds and methyl group 1,2-shift were also seen in some cases. Exceptional product ratios are observed for cross-reactions involving hydroxyalkyl radicals where H-bonding favors the homodimers in certain cases. Several bond strengths of C-H bonds α to CO were determined: EtCO2Me, 94.5; i-PrCO2Me, 92.7; cyclopentanone, 94.3; (i-Pr)2CO, 91.9 kcal/mol.

REDUCTIVE COUPLING OF α,β-ENONES PROMOTED BY Mg AND Mg-MgBr2

Pons, Jean-Marc,Santelli, Maurice

, p. 3679 - 3682 (2007/10/02)

α,β-enones able to have a s-cis conformation can be reduced by Mg (turnings 99.8percent) or more efficiently by Mg(99.8percent)-MgBr2, 10 Et2O in dimers (resulting from the formation of a bond between the Cβ carbon atoms) and dihydroketones.

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