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Trans-3,3-difluoro-1,2-dimethylcyclopropane is a cyclic hydrocarbon compound characterized by the presence of two fluorine atoms and two methyl groups. It has a unique structure with a three-carbon ring, where the fluorine atoms are attached to the same carbon atom (C3), and the methyl groups are attached to the other two carbon atoms (C1 and C2). trans-3,3-difluoro-1,2-dimethylcyclopropane is an example of a halogenated hydrocarbon, which is formed by the substitution of hydrogen atoms in a hydrocarbon molecule with halogen atoms. The trans configuration indicates that the fluorine atoms and methyl groups are positioned on opposite sides of the cyclopropane ring. trans-3,3-difluoro-1,2-dimethylcyclopropane may have potential applications in various fields, such as pharmaceuticals, agrochemicals, and materials science, due to its unique structure and properties.

338-01-2

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338-01-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 338-01-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,3 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 338-01:
(5*3)+(4*3)+(3*8)+(2*0)+(1*1)=52
52 % 10 = 2
So 338-01-2 is a valid CAS Registry Number.

338-01-2Relevant academic research and scientific papers

Aluminum oxide-induced gas-phase ring-opening in methyl substituted gem-difluorocyclopropanes, leading to 2-fluorobuta-1,3-dienes and vinylacetylenes

Volchkov,Lipkind,Novikov,Nefedov

, p. 658 - 663 (2015/11/27)

A gas-phase pyrolysis of methyl-substituted gem-difluorocyclopropanes in a flow-tube reactor in the presence of Al2O3 at 185 - 250 °C gives 2-fluorobuta-1,3-dienes and vinylacetylenes.

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