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2-(3-phenylsulfanylpropyl)cyclopentanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77516-32-6

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77516-32-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77516-32-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,5,1 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 77516-32:
(7*7)+(6*7)+(5*5)+(4*1)+(3*6)+(2*3)+(1*2)=146
146 % 10 = 6
So 77516-32-6 is a valid CAS Registry Number.

77516-32-6Relevant academic research and scientific papers

Synthesis of alkylated indolizidine alkaloids via Pummerer mediated cyclization: synthesis of (±)-indolizidine 167B, (±)-5-butylindolizidine and (±)-monomorine I

Kuhakarn, Chutima,Seehasombat, Phachanee,Jaipetch, Thaworn,Pohmakotr, Manat,Reutrakul, Vichai

, p. 1663 - 1670 (2008/09/17)

The syntheses of indolizidine alkaloids, i.e., (±)-coniceine, (±)-indolizidine 167B, (±)-5-butylindolizidine and (±)-monomorine I via Pummerer cyclization are described. The key step is the transformation of lactam sulfoxide to bicyclic lactam via the Pum

The preparation of synthetically useful carbonyl-protected δ- and ε-lithio ketones via reductive lithiation

Zhu, Shirong,Cohen, Theodore

, p. 17607 - 17624 (2007/10/03)

The aromatic radical-anion induced reductive lithiation of the acetals or thioacetals of δ- and ε-(phenylthio)ketones provides δ- and ε-lithioketone equivalents. Primary and tertiary organolithiums have been generated and the ketone function may be part o

Intramolecular Sulfur Ylide Additions to Ketones

Crandall, Jack K.,Magaha, H. Steve,Henderson, Mark A.,Widener, Rexford K.,Tharp, Gregg A.

, p. 5372 - 5380 (2007/10/02)

Methodology is described for the annulation of five-membered carboxylic rings onto cycloalkanones, using an intramolecular sulfur ylide reaction.Epoxybicycloalkanes (x = 3, 4, 5, 6) were obtained from cycloalkanones via the corresponding 2-3-(phen

INTRAMOLECULAR SULFOR-YLIDE ADDITIONS TO KETONES. A CYCLOPENTANE ANNULATION

Crandall, J. K.,Magaha, H. S.,,Widener, R. K.,Tharp, G. A.

, p. 4807 - 4810 (2007/10/02)

Various 2-(3'-phenylthiopropyl)cycloalkanones were prepared from the corresponding ketones and subjected to S-alkylation by triethyloxonium tetrafluoroborate followed by potassium tert-butoxide treatment to give bicyclic epoxides with new five-membered ca

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