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δ-(Butylsulfinyl)valerophenone is a chemical compound with the molecular formula C11H20OS. It is a derivative of valerophenone, featuring a butylsulfinyl group attached to the δ-carbon position. This organic compound is known for its unique properties, such as its ability to act as a chiral auxiliary in asymmetric synthesis, which can help in the creation of enantiomerically pure compounds. It is also used in the synthesis of various pharmaceuticals and agrochemicals due to its potential to influence the stereochemistry of reactions. The compound is characterized by its distinct smell and is typically handled with care due to its potential reactivity and toxicity.

66860-67-1

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66860-67-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66860-67-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,8,6 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 66860-67:
(7*6)+(6*6)+(5*8)+(4*6)+(3*0)+(2*6)+(1*7)=161
161 % 10 = 1
So 66860-67-1 is a valid CAS Registry Number.

66860-67-1Relevant academic research and scientific papers

Intramolecular Charge-Transfer Interactions in Triplet Keto Sulfides

Wagner, Peter J.,Lindstrom, Michael J.

, p. 3057 - 3062 (2007/10/02)

The photochemistry of β-,γ-and δ-phenacyl sulfides, sulfoxides, and sulfones has been studied.The first group undergoes no irreversible reaction.The other two undergo type II photoelimination but in low quantum efficiency.Analysis of triplet lifetimes and product quantum yields indicates that all undergo rapid internal quenching, which is ascribed to a charge-transfer (CT) process.The positional dependence of rate constants for this CT reaction is β > γ > α >> δ > ε .Some rate constants (units of 1E8 s-1) for PhCO(CH2)nSBu are as follows: n = 1, 16; n = 2, 55; n = 3, 29; n = 4 ,1.7; n = 5, PhS BuS(O) >> BuS, BuSO2, CH3CO-S and range from 1E9-3*1E5 s-1.Rate constants for triplet state γ-hydrogen abstraction were found to correlate well with the ?1 values of the various sulfur groups, except for δ-sulfinyl, which apparently participates in the reaction.

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