32804-07-2 Usage
Description
2-Chloro-3-fluoroprop-1-ene, with the molecular formula C3H4ClF, is a colorless liquid chemical compound characterized by a slightly sweet odor. It serves as a versatile intermediate in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals.
Uses
Used in Pharmaceutical Industry:
2-Chloro-3-fluoroprop-1-ene is used as a key intermediate in the synthesis of pharmaceuticals for its ability to be incorporated into complex molecular structures, contributing to the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 2-chloro-3-fluoroprop-1-ene is utilized as an intermediate in the production of various agrochemicals, such as pesticides and herbicides, due to its reactivity and potential to form effective active ingredients.
Safety Considerations:
Given its moderately toxic nature, 2-chloro-3-fluoroprop-1-ene can cause irritation to the skin, eyes, and respiratory system. Therefore, it is crucial to handle and store this compound with caution, adhering to proper safety protocols to minimize risks to human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 32804-07-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,8,0 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 32804-07:
(7*3)+(6*2)+(5*8)+(4*0)+(3*4)+(2*0)+(1*7)=92
92 % 10 = 2
So 32804-07-2 is a valid CAS Registry Number.
32804-07-2Relevant articles and documents
Preparation, fluorination and synthetic utility of a CFC-olefin adduct
Van Der Puy, Michael,Demmin, Timothy R.,Bindu Madhavan,Thenappan, Alagappan,Tung, Harry S.
, p. 49 - 54 (2007/10/03)
1,1,1-Trichlorotrifluoroethane was added to ethylene using the catalyst system Fe/triethylphosphite, which eliminated the need for a solvent and avoided the corrosion problems inherent in CuCl-catalyzed reactions. The adduct, CF3CCl2CH2CH2Cl, was fluorinated with HF over a chromium(III) oxide catalyst. A series of alternating dehydrochlorinations and HF additions to internal C=C double bonds was proposed and supported by thermodynamic calculations to explain the formation of CF3CF2CH=CH2 as the principal fluorination product. An intermediate, CF3CCl=CHCH2Cl, formed cleanly by dehydrochlorination of the adduct in the absence of HF, was converted into 4,4,4-trifluorobutanol and other compounds of the type CF3CCl=CHCH2X (X =OAc, OH, Br, I, H).
