141546-97-6 Usage
General Description
ETHYL 3-ETHOXY-2,2-DIFLUORO-3-HYDROXYPROPIONATE is a chemical compound with the molecular formula C6H10F2O4. It is a colorless liquid with a fruity odor, and is commonly used as a reagent in organic synthesis and pharmaceutical research. ETHYL 3-ETHOXY-2,2-DIFLUORO-3-HYDROXYPROPIONATE contains an ethoxy group, two difluoro groups, and a hydroxypropionate functional group, making it useful in various chemical reactions and processes. It is important to handle this chemical with care, as it may be harmful if swallowed or inhaled, and can cause skin and eye irritation if not handled properly. Overall, ETHYL 3-ETHOXY-2,2-DIFLUORO-3-HYDROXYPROPIONATE is a versatile compound with potential applications in many different fields of science and industry.
Check Digit Verification of cas no
The CAS Registry Mumber 141546-97-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,5,4 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 141546-97:
(8*1)+(7*4)+(6*1)+(5*5)+(4*4)+(3*6)+(2*9)+(1*7)=126
126 % 10 = 6
So 141546-97-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H12F2O4/c1-3-12-5(10)7(8,9)6(11)13-4-2/h5,10H,3-4H2,1-2H3
141546-97-6Relevant articles and documents
Synthesis of the fluorinated, phosphonated or sulfonated analogs of aspartic acid
Bijeire, Laurent,Denier, Colette,Mulliez, Michel,De Lima, Waldir Tavares
, p. 881 - 891 (2007/10/03)
Two stable hemiaminals, N acylated by the p-nitrobenzoyl or Boc group and each substituted by the difluorocarboxylethylester moiety, were obtained in a single step from the corresponding ethylhemiacetal. The Boc compound, after acylation by trifluoroaceti
Lewis Acid-Promoted Reaction of β,β-Difluorinated N,O-Acetal with Silylated Nucleophiles
Tsukamoto, Takashi,Kitazume, Tomoya
, p. 1377 - 1380 (2007/10/02)
Lewis acid-promoted reaction of ethyl 3-ethoxy-2,2-difluoro-3-(dimethylamino)propionate (1) with some silylated nucleophiles afforded β,β-difluoroamines in good yields.The formation of iminium ion intermediate from 1 and BF3*OEt2 was confirmed by 19F and 13C NMR spectroscopy.
