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α-Undecylcyclopentanone is a chemical compound with the molecular formula C16H28O, characterized by a cyclopentanone ring (a five-membered ring with a ketone group) and an undecyl chain (an 11-carbon alkyl chain). This organic molecule is known for its unique structure, which combines a cyclic ketone with a long alkyl chain. It is often used in the synthesis of various pharmaceuticals and chemical compounds due to its versatile chemical properties. The compound's structure allows it to participate in a range of reactions, such as nucleophilic addition to the ketone group and alkylation or acylation of the cyclopentanone ring. Its applications span across different industries, including the production of fragrances, agrochemicals, and specialty chemicals.

83019-13-0

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83019-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83019-13-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,0,1 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 83019-13:
(7*8)+(6*3)+(5*0)+(4*1)+(3*9)+(2*1)+(1*3)=110
110 % 10 = 0
So 83019-13-0 is a valid CAS Registry Number.

83019-13-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name α-undecylcyclopentanone

1.2 Other means of identification

Product number -
Other names 2-Undecyl-cyclopentanon

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:83019-13-0 SDS

83019-13-0Relevant academic research and scientific papers

STEREOSELECTIVE SYNTHESES OF SOLENOPSIN A AND B

Matsumura, Yasushi,Maruoka, Keiji,Yamamoto, Hisashi

, p. 1929 - 1932 (1982)

Effective and convenient syntheses of solenopsin A and B have been developed which involve the Beckmann rearrangement-alkylation reaction promoted by organoaluminum reagents and a new stereoselective reduction of imino functional group.

Two efficient four-step routes to marine toxin tanikolide

Chen, Qingshou,Deng, Haibing,Zhao, Jingrui,Lu, Yong,He, Mingyuan,Zhai, Hongbin

, p. 8390 - 8393 (2005)

We have presented two facile four-step syntheses of (±)-tanikolide from ethyl 2-oxocyclopentanecarboxylate. The overall chemical yields of the two sequences reached as high as 76 and 85%, respectively. The first strategy involved alkylation, Baeyer-Villiger reaction, saponification, and reduction/lactonization. The second approach for synthesizing tanikolide took advantage of the same intermediate, the alkylated ketoester 2, which was converted to the target molecule in such three steps as deethoxycarbonylation, hydroxymethylation, and Baeyer-Villiger reaction. Our strategies are advantageous because of their high yields and suitability for the preparation of 1 in multigram or larger quantities.

Organoaluminum-Promoted Beckmann Rearrangement of Oxime Sulfonates

Maruoka, Keiji,Miyazaki, Tohru,Ando, Mamoru,Matsumura, Yasushi,Sakane, Soichi,et al.

, p. 2831 - 2843 (2007/10/02)

The Beckmann rearrangement of oxime sulfonates with simultaneous nucleophilic trapping of the intermediary iminocarbocation by organoaluminum reagents is described.This process provides a new and highly efficient route to imino thioethers, imino selenoethers, imino nitriles, and α-alkylated amines starting from oxime sulfonates by the use of dialkylaluminum thiolates, selenolates, diethylaluminum chloride-trimethylsilyl cyanide, and trialkylaluminum-diisobutylaluminum hydride systems, respectively.The present organoaluminum-promoted Beckmann rearrangement of oxime sulfonates has been successfully applied to the synthesis of naturally occuring alkaloids, pumiliotoxin C and solenopsin A and B, in stereoselective fashion.Moreover, α,α-dialkylation of amines can be realized by the successive treatment of oxime sulfonates with trialkylaluminum followed by allylic or propargylic Grignard reagents in synthetically useful yields.

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