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3,3-difluoropentane is an organic compound with the molecular formula C5H10F2. It is a colorless, volatile liquid with a slight odor. This fluorinated alkane is characterized by the presence of two fluorine atoms attached to the same carbon atom in a pentane chain, which is a five-carbon straight chain. The fluorination of the molecule can significantly alter its physical and chemical properties compared to its non-fluorinated counterpart, pentane. 3,3-difluoropentane is used in various applications, including as a solvent, a chemical intermediate, and in the production of other fluorinated compounds. Due to its unique properties, it is also of interest in research for potential pharmaceutical and industrial applications.

358-03-2

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358-03-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 358-03-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,5 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 358-03:
(5*3)+(4*5)+(3*8)+(2*0)+(1*3)=62
62 % 10 = 2
So 358-03-2 is a valid CAS Registry Number.

358-03-2Downstream Products

358-03-2Relevant academic research and scientific papers

Transformation of Carbonyl Compounds into gem-Difluoro Compounds with Dibromodifluoromethane/Zinc Reagent

Hu, Chang-Ming,Qing, Feng-Ling,Shen, Cun-Xi

, p. 335 - 338 (2007/10/02)

Reaction of carbonyl compounds with dibromodifluoromethane/zinc gives the gem-difluoro compounds (12 examples).It seems to be that the reaction involves the generation of difluorocarbene by reaction of dibromodifluoromethane with zinc, followed by product

REACTIONS OF ALIPHATIC KETONES WITH SULFUR TETRAFLUORIDE AND HF IN THE PRESENCE OF SULFUR MONOCHLORIDE

Muratov, N.N.,Mohamed, Nagib Muhtar,Kunshenko, B.V.,Burmakov, A.I.,Alekseeva, L.A.,Yagupol'skii, L.M.

, p. 1292 - 1296 (2007/10/02)

Aliphatic ketones react with SF4 and anhydrous hydrogen fluoride in the presence of catalytic amounts of S2Cl2 to give polyfluorinated sulfides and disulfides.The reactions occur via intermediate alkene derivatives.

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