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5-Decyn-2-one, 4-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

141503-07-3

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141503-07-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141503-07-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,5,0 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 141503-07:
(8*1)+(7*4)+(6*1)+(5*5)+(4*0)+(3*3)+(2*0)+(1*7)=83
83 % 10 = 3
So 141503-07-3 is a valid CAS Registry Number.

141503-07-3Downstream Products

141503-07-3Relevant academic research and scientific papers

FeCl3-catalyzed nucleophilic substitution of propargylic acetates with enoxysilanes

Zhan, Zhuang-Ping,Cai, Xu-Bin,Wang, Shao-Pei,Yu, Jing-Liang,Liu, Hui-Juan,Cui, Yuan-Yuan

, p. 9838 - 9841 (2007)

(Chemical Equation Presented) An efficient FeCl3-catalyzed substitution reaction of propargylic acetates with enoxysilanes under mild conditions to afford corresponding γ-alkynyl ketones has been developed. The substitution reaction is followed

Copper(II) triflate-catalyzed nucleophilic substitution of propargylic acetates with enoxysilanes. A straightforward synthetic route to polysubstituted furans

Zhan, Zhuang-Ping,Wang, Shao-Pei,Cai, Xu-Bin,Liu, Hui-Juan,Yu, Jing-Liang,Cui, Yuan-Yuan

, p. 2097 - 2102 (2008/09/18)

A novel and efficient procedure for the synthesis of γ-alkynyl ketones by the nucleophilic substitution of propargylic acetates with enoxysilanes in the presence of a catalytic amount of Copper(II) triflate, has been developed. The substitution reaction c

Boron Trifluoride Etherate Mediated 1,4-Addition of (1-Alkynyl)diisopropoxyboranes to α,β-Unsaturated Ketones. A Convenient New Route to 3-Alkynyl Ketone Synthesis

Fujishima, Hiroaki,Takada, Ei-ichi,Hara, Shoji,Suzuki, Akira

, p. 695 - 698 (2007/10/02)

In the presence of BF3 etherate, (1-alkynyl)diisopropoxyboranes react with α,β-unsaturated ketones to give 1,4-addition products selectively in good yields.

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