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(1S,5R,6R,12R)-5-Methoxy-12-phenylsulfanyl-3-trimethylsilanyloxy-tricyclo[7.3.1.0^1,6]tridec-3-en-7-one is a complex organic compound with a unique molecular structure. It is characterized by a tricyclic ring system with a carbonyl group at the 7-position, a methoxy group at the 5-position, a phenylsulfanyl group at the 12-position, and a trimethylsilanyloxy group at the 3-position. (1S,5R,6R,12R)-5-Methoxy-12-phenylsulfanyl-3-trimethylsilanyloxy-tricyclo[7.3.1.01,6]tridec-3-en-7-one is a derivative of a tricyclic ketone, which is a type of organic molecule that contains a carbonyl group (C=O) within a cyclic structure. The specific stereochemistry of the compound, indicated by the (1S,5R,6R,12R) notation, describes the three-dimensional arrangement of the atoms at the chiral centers. The presence of the phenylsulfanyl group suggests potential applications in areas such as pharmaceuticals or materials science, where such functional groups can influence the compound's reactivity or physical properties. The trimethylsilanyloxy group may be used to protect the hydroxyl group or to facilitate certain chemical reactions. Overall, (1S,5R,6R,12R)-5-Methoxy-12-phenylsulfanyl-3-trimethylsilanyloxy-tricyclo[7.3.1.01,6]tridec-3-en-7-one represents a specific example of the vast diversity of organic chemistry, with potential applications depending on its specific properties and reactivity.

99656-30-1

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99656-30-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99656-30-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,6,5 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 99656-30:
(7*9)+(6*9)+(5*6)+(4*5)+(3*6)+(2*3)+(1*0)=191
191 % 10 = 1
So 99656-30-1 is a valid CAS Registry Number.

99656-30-1Downstream Products

99656-30-1Relevant academic research and scientific papers

Cycloaddition Reactions of Bridgehead Enones

Kraus, George A.,Hon, Yung-Son,Sy, James,Raggon, Jeff

, p. 1397 - 1400 (2007/10/02)

The cycloaddition reactions of bridgehead enones derived in situ from ketones 8,9, and 10 with various dienes at 0 deg C afford good yields of adducts.Even 1,1,3-trisubstituted dienes work well.The exclusive exo stereochemistry can be rationalized in term

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