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spiro[cyclohexane-1,2'-indan]-1'-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

26673-29-0

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26673-29-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26673-29-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,6,7 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 26673-29:
(7*2)+(6*6)+(5*6)+(4*7)+(3*3)+(2*2)+(1*9)=130
130 % 10 = 0
So 26673-29-0 is a valid CAS Registry Number.

26673-29-0Downstream Products

26673-29-0Relevant academic research and scientific papers

Synthesis of benzocyclic ketones via palladium-catalyzed cyclization of ω-(2-iodoaryl)alkanenitriles

Pletnev, Alexandre A.,Larock, Richard C.

, p. 2133 - 2136 (2002)

An efficient procedure for the synthesis of 2,2-disubstituted benzocyclic ketones by intramolecular carbopalladation of nitriles has been developed. The cyclization of substituted 3-(2-iodoaryl)propanenitriles affords indanones in high yields. The reactio

Carbopalladation of nitriles: Synthesis of benzocyclic ketones and cyclopentenones via Pd-catalyzed cyclization of ω-(2-iodoaryl)alkanenitriles and related compounds

Pletnev, Alexandre A.,Larock, Richard C.

, p. 9428 - 9438 (2007/10/03)

An efficient procedure for the synthesis of 2,2-disubstituted benzocyclic ketones by intramolecular carbopalladation of nitriles has been developed. The cyclization of substituted 3-(2-iodoaryl)-propanenitriles affords indanones in high yields. The reaction is compatible with a wide variety of functional groups. This methodology has been extended to the synthesis of tetralones and cyclopentenones.

Utilization of Bu3SnSiMe3 in organic synthesis II. New cyclization by a stannyl anion generated from Bu3SnSiMe3 and R4NX

Mori, Miwako,Kaneta, Naotake,Shibasaki, Masakatsu

, p. 35 - 40 (2007/10/02)

A new cyclization reaction of an aryl or vinyl halide bearing a carbonyl group such as ketone or ester has been developed by use of a stannyl anion generated in DMF from Bu3SnSiMe3 and Bu4NCl.Key words: Trimethylsilyl; Stannyl anion

Reaction of Metal Free Bu3Sn- Generated from Bu3SnSiMe3-R4NX with an Aryl or Vinyl Halide

Mori, Miwako,Kaneta, Naotake,Isono, Naoshiro,Shibasaki, Masakatsu

, p. 6139 - 6142 (2007/10/02)

Metal free stannyl anion generated from Bu3SnSiMe3 and R4NX in DMF reacted with an aryl or vinyl halide to produce the aryl or vinyl anion via so-called halogen-metal exchange process, which reacted with internal carbonyl group to afford cyclized product in good yield. Key Words: Bu3NSnSiMe3, Bu3Sn(1-)*R4N(1+), Metal free stannyl anion, Cyclization, Aryl or Vinyl anion

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