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N-(4-((2-methylbut-3-yn-2-yl)oxy)phenyl)acetamide is a complex organic compound with the molecular formula C13H15NO3. It is characterized by a phenyl ring (a six-carbon aromatic ring) with a 4-acetamide group attached, which is an amide derived from acetic acid. The unique feature of N-(4-((2-methylbut-3-yn-2-yl)oxy)phenyl)acetamide is the presence of a 2-methylbut-3-yn-2-yloxy group, which is a three-carbon chain with a methyl group and a terminal hydroxyl group, attached to the phenyl ring through an oxygen atom. This structure contributes to the compound's specific chemical properties and potential applications in various fields, such as pharmaceuticals or chemical research. The compound's exact uses and properties would depend on further study and experimentation, as its specific reactivity and interactions with other substances are not detailed in this summary.

2109-83-3

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2109-83-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2109-83-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,0 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2109-83:
(6*2)+(5*1)+(4*0)+(3*9)+(2*8)+(1*3)=63
63 % 10 = 3
So 2109-83-3 is a valid CAS Registry Number.

2109-83-3Relevant academic research and scientific papers

Copper-catalyzed intramolecular carbotrifluoromethylation of alkynes for the construction of trifluoromethylated heterocycles

Wang, Yanan,Jiang, Min,Liu, Jin-Tao

supporting information, p. 15315 - 15319 (2016/02/18)

A mild and efficient copper-catalyzed intramolecular carbotrifluoromethylation of alkynes has been achieved in the presence of Togni reagent as trifluoromethylating reagent. The reaction tolerates a range of substrates to give a group of trifluoromethylated heterocycles with high selectivities. A plausible mechanism was proposed on the basis of experimental results. And the Togni award goes to Copper-catalyzed intramolecular carbotrifluoromethylation of alkynes is carried out with a Togni reagent as the trifluoromethylating reagent (see scheme). Various trifluoromethylated heterocycles are synthesized in moderate to good yields. Moreover, a range of common functional groups is tolerated under the reaction conditions.

Asymmetric epoxidation of alkenes catalyzed by a porphyrin-inspired manganese complex

Dai, Wen,Li, Jun,Li, Guosong,Yang, Hua,Wang, Lianyue,Gao, Shuang

supporting information, p. 4138 - 4141 (2013/09/12)

A novel strategy for catalytic asymmetric epoxidation of a wide variety of olefins by a porphyrin-inspired chiral manganese complex using H 2O2 as a terminal oxidant in excellent yield with up to greater than 99% ee has been successfully developed.

Improved Synthesis of Aryl 1,1-Dimethylpropargyl Ethers

Godfrey, Jollie D.,Mueller, Richard H.,Sedergran, Thomas C.,Soundarajan, Nachimuthu,Colandrea, Vincent J.

, p. 6405 - 6408 (2007/10/02)

An efficient, general, and practical synthesis of aryl 1,1-dimethylpropargyl ethers has been developed.

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