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The chemical compound "(3aR*,4R*,7aR*)-3a-ethoxycarbonyl-4-methoxy-2,3,6-trioxo-7a-phenyl-1-trimethylsilyloxy-2,3,3a,4,5,6,7,7a-octahydroindole" is a complex organic molecule with a unique structure. It features an octahydroindole core, which is a type of indole ring system that has been fully saturated, meaning all the double bonds have been reduced to single bonds. The compound is characterized by the presence of several functional groups, including an ethoxycarbonyl group at the 3a position, a methoxy group at the 4 position, and a trimethylsilyloxy group at the 1 position. Additionally, it has a phenyl group attached at the 7a position and three carbonyl groups at the 2, 3, and 6 positions. This molecule is a chiral compound, with the specified stereochemistry at the 3a, 4, and 7a positions being R*, indicating that the substituents at these centers are arranged in a specific three-dimensional orientation. The compound's structure and properties make it a potential candidate for various applications in the fields of pharmaceuticals, materials science, and organic chemistry, particularly in the synthesis of complex natural products and the development of new drugs.

86236-61-5

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86236-61-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86236-61-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,2,3 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 86236-61:
(7*8)+(6*6)+(5*2)+(4*3)+(3*6)+(2*6)+(1*1)=145
145 % 10 = 5
So 86236-61-5 is a valid CAS Registry Number.

86236-61-5Downstream Products

86236-61-5Relevant academic research and scientific papers

FACTORS CONTROLLING C=C VS. C=O ATTACK IN CYCLOADDITION OF A 1,3-DIENE TO AN AMBIDENT DIENOPHILE. DIELS-ALDER REACTION OF 2-PHENYL-Δ2-PYRROLINE-4,5-DIONES

Sano, Takehiro,Toda, Jun,Tsuda, Yoshisuke

, p. 356 - 359 (2007/10/02)

The cycloaddition using an enone as a dienophile is on a balance with the normal C=C attack (ene-addition) and the unusual C=O attack (one-addition) of a diene.Steric hindrance on the C=C (caused by such phenomena as restricted free rotation of the substituent on C=C) retards the C=C attack, thus increasing the ratio of one-addition.Lewis acids greatly increase not only the reactivity of C=O but also the ratio of one-addition.KEYWORDS --- 1-methoxy-3-trimethylsilyloxybutadiene; Diels-Alder reaction; dioxopyrroline; ambident dienophile; ene-addition; one-addition; steric hindrance; Lewis acid

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