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2-((4-phenylbut-3-yn-2-yl)oxy)ethanol is an organic compound characterized by a unique molecular structure. It features a central ethanol moiety, which is an alcohol with two hydroxyl groups attached to a two-carbon chain. One of the hydroxyl groups is connected to a but-3-yn-2-yl group, which is a four-carbon chain with a triple bond between the third and fourth carbon atoms, and a phenyl group attached to the fourth carbon. The phenyl group, in turn, is a benzene ring, which is a stable aromatic structure. The other hydroxyl group is connected to an ethereal oxygen atom, forming an ether linkage. 2-((4-phenylbut-3-yn-2-yl)oxy)ethanol is notable for its combination of hydroxyl, ether, and alkyne functionalities, which can contribute to its reactivity and potential applications in chemical synthesis and as a building block for more complex molecules.

6738-08-5

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6738-08-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6738-08-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,3 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6738-08:
(6*6)+(5*7)+(4*3)+(3*8)+(2*0)+(1*8)=115
115 % 10 = 5
So 6738-08-5 is a valid CAS Registry Number.

6738-08-5Downstream Products

6738-08-5Relevant articles and documents

Catalytic Alkynylation of Cyclic Acetals and Ketals Enabled by Synergistic Gold(I)/Trimethylsilyl Catalysis

Berthet, Mathéo,Songis, Olivier,Taillier, Catherine,Dalla, Vincent

, p. 9916 - 9922 (2017)

A completely regioselective and challenging gold(I)-catalyzed ring-opening of cyclic 1,3-dioxolanes and dioxanes by trimethylsilyl alkynes to set diol-derived propargyl trimethylsilyl bis-ethers is reported. This unprecedented and not trivial transformation does not operate with the catalytic methodologies recently reported for catalytic alkynylation of acyclic acetals/ketals, and is uniquely enabled by the application of a recently introduced synergistic gold(I)-silicon catalysis concept capable of producing simultaneously catalytic amounts of two key players, a silicon-based Lewis superacid and a nucleophilic gold acetylide.

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