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1,1'-Dimethylethenebisallene, also known as 1,1'-dimethyl-2,2'-(1,2-ethenediyl)bisallene, is an organic compound with the chemical formula C8H10. It is a symmetrical molecule consisting of two allene units connected by a central ethene bridge, with a methyl group attached to each allene unit. 1,1'-Dimethylethenebisallene is of interest in organic chemistry due to its unique structure and potential applications in the synthesis of more complex molecules. It is typically synthesized through various chemical reactions and can be used as a building block for the creation of other organic compounds. The study of 1,1'-dimethylethenebisallene contributes to the understanding of the properties and reactivity of allene-containing molecules, which are important in the field of organic synthesis.

4356-63-2

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4356-63-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4356-63-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,5 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4356-63:
(6*4)+(5*3)+(4*5)+(3*6)+(2*6)+(1*3)=92
92 % 10 = 2
So 4356-63-2 is a valid CAS Registry Number.

4356-63-2Upstream product

4356-63-2Downstream Products

4356-63-2Relevant academic research and scientific papers

Some Reactions and Properties of Molecular C2. An Experimental and Theoretical Treatment

Skell, Philip S.,Jackman, Lloyd M.,Ahmed, Sheikh,McKee, Michael L.,Shevlin, Philip B.

, p. 4422 - 4429 (1989)

Diatomic carbon, C2, reacts with propylene and (E)- and (Z)-2-butene in the condensed phase at 77 K.Products can be rationalized by a mechanism involving initial addition of C2 to the alkene to generate a 1,4-diradical.This diradical may then either abstract hydrogens or add another alkene molecule to give a 1,6-diradical which disproportionates to an enyne.Thus, reaction of C2 with propene gives 1-pentyne, 3-methyl-1-butyne, 4-methylhept-6-en-1-yne, 6-methylhept-1-en-4-yne, and oct-1-en-4-yne.Ab initio calculations at the HF/3-21G level predict that both 1C2 and 3C2 will add to ethylene without barrier.At the MP2/6-31G*//3-21G level, the triplet adduct is calculated to be more stable than 3C2 and ethylene by 46.0 kcal/mol.The reactions of 1C2 and 3C2 with methane and hydrogen have also been investigated theoretically.

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