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δ-(Thioacetoxy)valerophenone, also known as 4-(thioacetoxy)valeric acid phenylmethyl ester, is an organic compound with the chemical formula C11H14O2S. It is a colorless to pale yellow liquid with a molecular weight of 210.29 g/mol. δ-(Thioacetoxy)valerophenone is primarily used as a synthetic intermediate in the production of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is characterized by its unique thioester functional group, which makes it a valuable building block in organic synthesis. The compound is sensitive to heat and moisture, and it is typically stored under cool, dry conditions to maintain its stability.

66860-72-8

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66860-72-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66860-72-8 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, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 66860-72:
(7*6)+(6*6)+(5*8)+(4*6)+(3*0)+(2*7)+(1*2)=158
158 % 10 = 8
So 66860-72-8 is a valid CAS Registry Number.

66860-72-8Downstream Products

66860-72-8Relevant academic research and scientific papers

Intramolecular Charge-Transfer Interactions in Triplet Keto Sulfides

Wagner, Peter J.,Lindstrom, Michael J.

, p. 3057 - 3062 (1987)

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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