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The chemical compound "(3aR*,4S*,7aR*)-3a-ethoxycarbonyl-4-methoxy-1-methyl-2,3,6-trioxo-7a-phenyl-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 in the indole have been reduced to single bonds. The compound is characterized by the presence of an ethoxycarbonyl group at the 3a position, a methoxy group at the 4 position, and a methyl group at the 1 position. Additionally, it has three carbonyl groups at the 2, 3, and 6 positions, and a phenyl group at the 7a position. The stereochemistry is specified by the R* configuration the at 3a, 4, and 7a positions, indicating that the substituents at these centers are arranged in a specific three-dimensional orientation. (3aR*,4S*,7aR*)-3a-ethoxycarbonyl-4-methoxy-1-methyl-2,3,6-trioxo-7a-phenyl-2,3,3a,4,5,6,7,7a-octahydroindole is likely to be of interest in the field of organic chemistry, potentially for its pharmacological properties or as a synthetic intermediate in the preparation of more complex molecules.

86236-62-6

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86236-62-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86236-62-6 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 86236-62:
(7*8)+(6*6)+(5*2)+(4*3)+(3*6)+(2*6)+(1*2)=146
146 % 10 = 6
So 86236-62-6 is a valid CAS Registry Number.

86236-62-6Downstream Products

86236-62-6Relevant 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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