460-36-6 Usage
General Description
1,1,1,3-Tetrafluoropropane is a type of chemical compound more commonly known as HFC-134a. It's primarily used as a refrigerant for air conditioning and refrigeration. This chemical has been vital in the transition away from harmful chlorofluorocarbons (CFCs) which were found to be responsible for the depletion of the ozone layer. Although it has a significantly lower ozone depletion potential compared to its predecessors, it's not completely environmentally harmless, as it is a potent greenhouse gas with a global warming potential over 1,000 times that of carbon dioxide. As such, despite its initial introduction as an environmentally friendly alternative, its use is now being phased out in many countries in favor of substances with lower global warming potentials.
Check Digit Verification of cas no
The CAS Registry Mumber 460-36-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,6 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 460-36:
(5*4)+(4*6)+(3*0)+(2*3)+(1*6)=56
56 % 10 = 6
So 460-36-6 is a valid CAS Registry Number.
InChI:InChI=1/C3H4F4/c4-2-1-3(5,6)7/h1-2H2
460-36-6Relevant articles and documents
Versatile Reaction Pathways of 1,1,3,3,3-Pentafluoropropene at Rh(I) Complexes [Rh(E)(PEt3)3] (E=H, GePh3, Si(OEt)3, F, Cl): C-F versus C-H Bond Activation Steps
Braun, Thomas,Talavera, Maria
supporting information, p. 11926 - 11934 (2021/07/06)
The reaction of the rhodium(I) complexes [Rh(E)(PEt3)3] (E=GePh3 (1), H (6), F (7)) with 1,1,3,3,3-pentafluoropropene afforded the defluorinative germylation products Z/E-2-(triphenylgermyl)-1,3,3,3-tetrafluoropropene and
REACTION OF HYDROXY AND CARBONYL COMPOUNDS WITH SULFUR TETRAFLUORIDE. X. REACTION OF ALIPHATIC β-HYDROXYCARBOXYLIC ACIDS WITH SULFUR TETRAFLUORIDE
Motnyak, L. A.,Burmakov, A. I.,Kunshenko, B. V.,Neizvestnaya, T. A.,Alekseeva, L. A.,Yagupol'skii, L. M.
, p. 634 - 640 (2007/10/02)
The reactions of 3-hydroxypropionic, d,l-3-hydroxybutyric, d,l-4,4,4-trifluoro-3-hydroxybutyric, and 4,4,4-trifluoro-3-trifluoromethyl-3-hydroxybutyric acids with sulfur tetrafluoride were investigated.It was shown that the electronic nature of the substituents at the β-carbon atom has a significant effect on the direction of the reactions of β-hydroxycarboxylic acids with sulfur tetrafluoride.
