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3,3-difluoro-1,4-pentadiene is a colorless liquid organic compound with the molecular formula C5H6F2. It is a conjugated diene, which means it has two carbon-carbon double bonds separated by a single bond. The presence of two fluorine atoms at the 3,3-position of the pentadiene structure imparts unique chemical properties to the molecule. 3,3-difluoro-1,4-pentadiene is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. Due to its reactivity, it is often employed in Diels-Alder reactions, a type of cycloaddition reaction that forms six-membered rings. The compound is also known for its potential use in the production of polymers and as a building block for more complex organic molecules. It is important to handle 3,3-difluoro-1,4-pentadiene with care due to its potential reactivity and sensitivity to certain conditions.

380-55-2

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380-55-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 380-55-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,8 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 380-55:
(5*3)+(4*8)+(3*0)+(2*5)+(1*5)=62
62 % 10 = 2
So 380-55-2 is a valid CAS Registry Number.

380-55-2Downstream Products

380-55-2Relevant academic research and scientific papers

THE THERMAL DEAZETATIONS OF FLUORINATED 2,3-DIAZABICYCLOHEPT-2-ENES

Dolbier, William R.,Al-Pekri, Dheya M.

, p. 39 - 44 (2007/10/02)

Thermal deazetation of difluoro- and tetrafluoro-2,3-diazabicyclohept-2-enes proceed via two parallel mechanistic pathways, one involving formation of a diradical via simple N2 loss, and the other proceeding via a retro-dipolar cycloaddition process.A key finding was the absence of isolation of a bicyclopentane product in the difluoro case.

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