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<2-Methyl-hexyl-(3)>-tosylat is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92372-39-9

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92372-39-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92372-39-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,3,7 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 92372-39:
(7*9)+(6*2)+(5*3)+(4*7)+(3*2)+(2*3)+(1*9)=139
139 % 10 = 9
So 92372-39-9 is a valid CAS Registry Number.

92372-39-9Downstream Products

92372-39-9Relevant academic research and scientific papers

Efficient and mild Ytterbium(III)-catalyzed tosylation of alcohols

Comagic, Slobodan,Schirrmacher, Ralf

, p. 885 - 888 (2004)

Ytterbium(III) trifluoromethanesulfonate efficiently catalyzes the reaction of primary and secondary alcohols with toluenesulfonic acid anhydride to yield the alkyl tosylates in high yields. The reactions were carried out under neutral and mild conditions and product purification was easily achieved by means of short column chromatography.

Structure-odor correlations in homologous series of alkanethiols and attempts to predict odor thresholds by 3d-qsar studies

Polster, Johannes,Schieberle, Peter

, p. 1419 - 1432 (2015/03/05)

Homologous series of alkane-1-thiols, alkane-2-thiols, alkane-3-thiols, 2-methylalkane-1-thiols, 2-methylalkane-3-thiols, 2-methylalkane-2-thiols, and alkane-1,??-dithiols were synthesized to study the influence of structural changes on odor qualities and odor thresholds. In particular, the odor thresholds were strongly influenced by steric effects: In all homologous series a minimum was observed for thiols with five to seven carbon atoms, whereas increasing the chain length led to an exponential increase in the odor threshold. Tertiary alkanethiols revealed clearly lower odor thresholds than found for primary or secondary thiols, whereas neither a second mercapto group in the molecule nor an additional methyl substitution lowered the threshold. To investigate the impact of the SH group, odor thresholds and odor qualities of thiols were compared to those of the corresponding alcohols and (methylthio)alkanes. Replacement of the SH group by an OH group as well as S-methylation of the thiols significantly increased the odor thresholds. By using comparative molecular field analysis, a 3D quantitative structure-activity relationship model was created, which was able to simulate the odor thresholds of alkanethiols in good agreement with the experimental results. NMR and mass spectrometric data for 46 sulfur-containing compounds are additionally supplied.

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