356-36-5 Usage
General Description
DIMETHYL TETRAFLUOROSUCCINATE is a chemical compound with the molecular formula C6H8F4O4. It is a white crystalline solid that is used as a reagent in organic synthesis and as a building block for various pharmaceuticals and agrochemicals. DIMETHYL TETRAFLUOROSUCCINATE is also known for its ability to act as a fluorinating agent, introducing fluorine atoms into organic molecules. It is considered to be a stable and non-reactive compound, making it useful for a variety of chemical reactions. Additionally, it is important to handle DIMETHYL TETRAFLUOROSUCCINATE with care as it can be toxic if ingested and may cause irritation upon contact with skin or eyes.
Check Digit Verification of cas no
The CAS Registry Mumber 356-36-5 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 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 356-36:
(5*3)+(4*5)+(3*6)+(2*3)+(1*6)=65
65 % 10 = 5
So 356-36-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H6F4O4/c1-13-3(11)5(7,8)6(9,10)4(12)14-2/h1-2H3
356-36-5Relevant articles and documents
Ozonolysis of alkenes and studies of reactions of polyfunctional compounds: LXIII.* Ozonolysis of 2,3,3,4,4,-pentafluoro-1-methoxycyclobutene
Odinokov,Akhmetova,Savchenko,Bazunova,Paramonov,Khalilov
, p. 1437 - 1445 (2007/10/03)
Ozonolysis of 2,3,4,4-pentafluoro-1-methoxycyclobutene in Freon-113 leads to formation of cyclic products containing eight fluorine atoms. Ozonolysis of the same compound in Freon-113 in the presence of alcohols yields the corresponding alkyl methyl perfluorosuccinate.
ALDOL REACTION OF IODODIFLUOROACETATE-Zn AND 2,2-DIFLUOROKETENE SILYL ACETAL
Kitagawa, Osamu,Taguchi, Takeo,Kobayashi, Yoshiro
, p. 1803 - 1806 (2007/10/02)
Generation of the Reformatsky reagent of difluoroacetate from the iodide(2) and the difluoroketene silyl acetal(3), and their aldol reaction are described.High anti-selectivity with chiral aldehyde (5d, 5f) was found in the case of the ketene silyl acetal(3b). 2,2-Difluoro-2-deoxy analogs of D-ribo- and L-galactopyranosides (1a, 1b) were effectively prepared.
