460-60-6 Usage
Uses
Used in Fire Suppression:
1,3-DIBROMO-1,1,3-TRIFLUOROPROPANE is used as a fire suppressant due to its ability to effectively control and extinguish fires. Its non-flammable nature and reactivity make it a suitable candidate for this application.
Used in Refrigeration:
This chemical compound serves as a refrigerant in various cooling systems, leveraging its properties to maintain low temperatures for preservation and cooling purposes.
Used in Pharmaceutical Production:
1,3-DIBROMO-1,1,3-TRIFLUOROPROPANE is used as a solvent in the synthesis of pharmaceuticals, contributing to the manufacturing process of various medicinal compounds.
Used in Organic Compound Synthesis:
It is also utilized as a solvent in the production of other organic compounds, facilitating chemical reactions that are essential in the synthesis of a range of products.
However, due to the potential for skin, eye, and respiratory irritation, as well as the risk of damage to the central nervous system and other organs from long-term exposure, the use of 1,3-DIBROMO-1,1,3-TRIFLUOROPROPANE must be carefully managed to minimize risks to human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 460-60-6 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, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 460-60:
(5*4)+(4*6)+(3*0)+(2*6)+(1*0)=56
56 % 10 = 6
So 460-60-6 is a valid CAS Registry Number.
InChI:InChI=1/C3H3Br2F3/c4-2(6)1-3(5,7)8/h2H,1H2
460-60-6Relevant academic research and scientific papers
Processes for synthesis of 1,3,3,3-tetrafluoropropene
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Page/Page column 4, (2008/06/13)
Disclosed is a process for the synthesis of 1,3,3,3-tetrafluoropropene that comprises, in one preferred embodiment, providing a compound of the formula CF3CH2CHFX, wherein X is a selected from the group consisting of chlorine, bromine and iodine, and exposing said compound to reaction conditions effective to convert said compound to 1,3,3,3-tetrafluoropropene. Other processes for forming 1,3,3,3-tetrafluoropropene are also disclosed.
