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2,2,6,6-Tetramethyl-cyclohexanecarbothioic acid O-methyl ester is a chemical compound with the molecular formula C11H22OS. It is a derivative of cyclohexane, featuring a sulfur atom bonded to a carbonyl group, which is further esterified with a methyl group. 2,2,6,6-Tetramethyl-cyclohexanecarbothioic acid O-methyl ester is characterized by its tetrahedral structure due to the presence of the sulfur atom and its ability to form thioesters. It is an organic compound that can be used in various chemical reactions and synthesis processes, particularly in the preparation of pharmaceuticals and agrochemicals. The compound's structure provides it with unique chemical properties, such as its reactivity towards nucleophiles and its potential to act as a ligand in coordination chemistry.

98687-87-7

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98687-87-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98687-87-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,6,8 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 98687-87:
(7*9)+(6*8)+(5*6)+(4*8)+(3*7)+(2*8)+(1*7)=217
217 % 10 = 7
So 98687-87-7 is a valid CAS Registry Number.

98687-87-7Downstream Products

98687-87-7Relevant academic research and scientific papers

Photochemical Behavior of Thioketenes in Solution: Reaction from S2

Singh, Sharat,Nimmesgern, Hildegard,Schaumann, Ernst,Ramamurthy, Vaidhyanathan

, p. 4799 - 4805 (2007/10/02)

The higher excited-state reactions of sterically encumbered thioketenes 1a-d in solution were investigated.Substituted thiiranes, thio esters, thioacetophenones, and 1,2-diones are formed on photoexcitation of thioketenes in hydroxylic and nonhydroxylic solvents.Thioketenes while unreactive upon excitation to S1 produce thiiranylidene carbene and zwitterionic intermediates upon excitation to S2.The reactive state is identified to be S2 (??*).The excited thioketene resists carbon monosulfide elimination but undergoes rearrangement.The photobehavior of thioketenes, established in solution for the first time, differs significantly from that of ketenes, and it cannot be extrapolated from that of structurally analogous ketenes and allenes.

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