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2-Bromo-1,1-difluorocyclopropane is a halogenated cyclopropane derivative, featuring a three-carbon cyclic structure with a bromine atom at the 2-position and two fluorine atoms at the 1-position. This organic compound is characterized by its unique molecular structure, which contributes to its distinct chemical properties and potential applications. It is a colorless liquid with a high reactivity due to the presence of both bromine and fluorine atoms, making it a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. The compound's stability and reactivity can be influenced by factors such as temperature, pressure, and the presence of other reactive species, highlighting the importance of controlled conditions during its handling and use.

51326-64-8

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51326-64-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51326-64-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,3,2 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 51326-64:
(7*5)+(6*1)+(5*3)+(4*2)+(3*6)+(2*6)+(1*4)=98
98 % 10 = 8
So 51326-64-8 is a valid CAS Registry Number.

51326-64-8Downstream Products

51326-64-8Relevant academic research and scientific papers

Reduction of fluorinated cyclopropene by nitrogenase

Ni, Feng,Lee, Chi Chung,Hwang, Candy S.,Hu, Yilin,Ribbe, Markus W.,Mckenna, Charles E.

supporting information, p. 10346 - 10352 (2013/08/23)

Reduction of the first known halogen-containing substrate by nitrogenase (N2ase), 3,3-difluorocyclopropene (DFCP), was investigated. Reduction requires both N2ase proteins (MoFe and Fe protein), ATP, and an exogenous reductant (dithionite, DT), as with N2 and known alternative substrates of the enzyme. Two major products providing evidence for reductive C-F bond cleavage were confirmed, propene (P1, requiring 6e -/6H+) and 2-fluoropropene (P2, 4e-/4H +). Both were identified by GC-MS and NMR spectroscopy, and had the same Km constants (0.022 atm, 5.4 mM). Reduction of 1,2-dideuterated DFCP (d2-DFCP) further revealed that (i) in both P1 and P2, two deuterium atoms are retained, one on carbon-1 and one on carbon-3, indicating that C=C bond cleavage rather than C-C bond cleavage is involved during DFCP reduction at least to P2 (assuming no F migration); (ii) no selectivity was observed in formation of cis and trans isomers of 1,3-d2-2- fluoropropene, whereas cis-1,3-d2-propene is the predominant 1,3-d2-propene product, indicating that one of the bound reduction intermediates on the pathway to propene is constrained geometrically. A reduction mechanism, consistent with hydride transfer as a key step, is discussed. Reductive C-F bond cleavage is an ability of N2ase that further demonstrates the unique and remarkable scope of its catalytic prowess.

CYCLOPROPANE CHEMISTRY. PART 5 . HEXAFLUOROCYCLOPROPANE AS A SOURCE OF DIFLUOROCARBENE

Birchall, J. Michael,Fields, Roy,Haszeldine, Robert N.,McLean, Reginald J.

, p. 487 - 496 (2007/10/02)

Thermolysis of hexafluorocyclopropane in the presence of ethylene, propene, vinyl chloride, and vinyl bromide gives good yields of the corresponding 1,1-difluorocyclopropanes, formed by addition of difluorocarbene to the olefin.The tetrafluoroethylene formed dimerises to octafluorocyclobutane, co-dimerises with the olefin, or survives, depending on the reaction conditions.With allene, hexafluorocyclopropane gives 1-(difluoromethylene)cyclopropane, 2,2,3,3-tetrafluorospiropentane, and products derived from tetrafluoroethylene and allene.

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