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(2R,3'R)-1'-Benzyl-2-(2-methyl-[1,3]dioxolan-2-ylmethyl)-1,2-dihydro-spiro[indole-3,3'-pyrrolidine]-2',5'-dione is a complex organic compound with a unique molecular structure. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it is characterized by the presence of a benzyl group, a 2-methyl-[1,3]dioxolan-2-ylmethyl group, and a spiro[indole-3,3'-pyrrolidine] core. The compound features a 1,2-dihydro system, indicating the presence of two hydrogen atoms bonded to a carbon atom, and a 2',5'-dione group, which consists of two carbonyl groups. This chemical is likely to be found in specialized applications due to its intricate structure, potentially in the field of pharmaceuticals or as an intermediate in the synthesis of other complex molecules.

88686-80-0

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88686-80-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88686-80-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,6,8 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 88686-80:
(7*8)+(6*8)+(5*6)+(4*8)+(3*6)+(2*8)+(1*0)=200
200 % 10 = 0
So 88686-80-0 is a valid CAS Registry Number.

88686-80-0Downstream Products

88686-80-0Relevant academic research and scientific papers

Diastereoselective photochemical synthesis of 3,3'-disubstituted indolines

Ibrahim-Ouali, Malika,Sinibaldi, Marie-Eve,Troin, Yves,Guillaume, Dominique,Gramain, Jean-Claude

, p. 16083 - 16096 (2007/10/03)

Spiroindoline lactams 9 and imides 11 were efficiently and diastereoselectively prepared by photocyclization of N-arylenaminolactams 8 and esters 5 respectively. Imides 11 wee conveniently transformed into the known indolines 13 and 14 which are key intermediates for the synthesis of (±)-vindorosine and Aspidosperma alkaloids.

STEREOCONTROLLED FORMATION OF 1,2-DIHYDROINDOLES

Veenstra, S.J.,Fortgens, H.P.,Vijn, R.J.,Jong, B.S. de,Speckamp, W.N.

, p. 1147 - 1156 (2007/10/02)

Imines 4 cyclize stereoselectively to dihydroindoles 2 upon use of a Li or Na alkoxide-alcohol combination.Depending on the type of alcohol applied either cis (2C) or trans (2T) spiroindolines 2 are formed.In case of imines 4 derived from electron-rich ar

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