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α-Fluor-zimtsaeurediethylamid, also known as α-fluorocitronic acid diethylamide, is a chemical compound with the molecular formula C10H16FNO4. It is a derivative of citric acid, featuring a fluorine atom at the α-position and two ethylamine groups attached to the remaining hydroxyl groups. α-Fluor-zimtsaeurediethylamid is of interest in the field of organic chemistry, particularly in the study of fluorinated organic compounds, which often exhibit unique reactivity and properties compared to their non-fluorinated counterparts. α-Fluorocitronic acid diethylamide may be used in the synthesis of various pharmaceuticals and agrochemicals, as well as in the development of new materials with specific properties. Its synthesis typically involves the protection of citric acid's hydroxyl groups, followed by fluorination and subsequent deprotection to yield the final product.

55305-87-8

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55305-87-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55305-87-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,3,0 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 55305-87:
(7*5)+(6*5)+(5*3)+(4*0)+(3*5)+(2*8)+(1*7)=118
118 % 10 = 8
So 55305-87-8 is a valid CAS Registry Number.

55305-87-8Downstream Products

55305-87-8Relevant academic research and scientific papers

Short, stereoselective syntheses of α-fluoroalkenoate derivatives, α- fluoroenones and α-fluoroenals from HFC-134a

Kanai,Percy

, p. 2453 - 2455 (2000)

Readily-available 1,1,1,2-tetrafluoroethane (Klea HFC-134a) can be converted, via a two-pot sequence into a range of Z-α-fluoroalkenoyl derivatives following addition reactions to aldehydes. Reaction adducts can be processed into enals and enones upon hydride reduction or Grignard reagent addition in high yield. (C) 2000 Elsevier Science Ltd.

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