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(3,5,6-tris((trimethylsilyl)ethynyl)benzene-1,2,4-triyl)tris(trimethylsilane) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18765-46-3

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18765-46-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18765-46-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,7,6 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 18765-46:
(7*1)+(6*8)+(5*7)+(4*6)+(3*5)+(2*4)+(1*6)=143
143 % 10 = 3
So 18765-46-3 is a valid CAS Registry Number.

18765-46-3Relevant academic research and scientific papers

Chemoselective Cobalt(I)-Catalyzed Cyclotrimerization of (Un)Symmetrical 1,3-Butadiynes for the Synthesis of 1,2,4-Regioisomers

Weber, Sebastian M.,Hilt, Gerhard

supporting information, p. 4106 - 4110 (2019/06/17)

The cobalt(I)-catalyzed cyclotrimerization of (un)symmetrical 1,4-disubstituted 1,3-butadiynes is presented. In the case of unsymmetrical 1,3-butadiynes, this reaction can generate eight 1,2,4-substituted and four 1,3,5-substituted isomers. A single 1,2,4-substituted isomer was formed in excellent yields (up to 99%) and exclusive regioselectivities (>99:1) when symmetrical or a 1,3-butadiyne with an aryl or alkyl substituent and a trimethylsilyl group were applied. A large number of products accepting a wide variety of functional groups were synthesized.

The diethynylcyclobutadlene rearrangement: A degenerate ligand reorganization in the coordination sphere of (η5-Cyclopentadlenyl) cobalt

Fritch, Jonn R.,Volhardt, K. Peter C.

, p. 590 - 602 (2008/10/08)

Reaction of CpCo(CO)2 with bis(trimethylsilyl)butadiyne leads lo small amounts of silyleted 1,2- and 1,3-diethynylcyclobutadiene compleses 13 and 18 among other products. Alternatively, cocyclization of bis(trimethylsilyl)hexatriyne with bis(trimethylsilyl)acetylene furnishes 13 in 64.2% yield. These compounds may be protodesilylated with alcoholic KOH or fluoride. Flash vacuum thermolysis of the 1,2-diethynylcyclobutadiene complexes 9, 19, and 49 induces a clean rearrangement in which the four sp carbons of the ethynyl groups cyclize to form a new cyclobutadiene ring and the original cyclobutadiene ring retrocyclizes to generate two new alkyne groups. In this way 9 undergoes a degenerate rearrangement, whereas 19 converts to 30, and 49 equilibrates with 50. Mechanistic speculation is offered which suggests a CpCo-complexed cycloocta-3,7-diene-1,5-diyne (11) or cycloocta-1,2,3,5,6,7-hexaene (12) as a likely intermediate, A topologically equivalent alternnative, (η4-tricyclo[4,2.0.0 2,5]octs-1,3,5,7-tetraene)(η5-cyclopentadienyl)cobalt (10), appears less favored on theoretical grounds.

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