141535-83-3 Usage
Explanation
This is the IUPAC name of the compound, which provides information about the structure and functional groups present in the molecule.
Explanation
The compound is known for its high reactivity, which makes it useful in various chemical reactions and industrial processes.
Explanation
Due to its high reactivity, 1-Butene, 1,1-dichloro-2,3,4,4,4-pentafluoro- is also flammable, which means it can easily catch fire when exposed to a source of ignition.
Explanation
The compound is used in various industries, including the production of polymers and plastics, as a refrigerant, and in the manufacture of foam-blowing agents.
Explanation
1-Butene, 1,1-dichloro-2,3,4,4,4-pentafluorois considered a hazardous chemical due to its potential health and environmental risks.
Explanation
Exposure to 1-Butene, 1,1-dichloro-2,3,4,4,4-pentafluoro- can lead to respiratory problems and skin irritation, emphasizing the need for proper handling and safety precautions.
Explanation
Due to its hazardous nature, it is essential to handle 1-Butene, 1,1-dichloro-2,3,4,4,4-pentafluoro- with caution, using appropriate personal protective equipment (PPE) and following safety guidelines.
Reactivity
Highly reactive
Flammability
Flammable
Applications
Production of polymers and plastics, refrigerant, foam-blowing agents
Hazardous
Yes
Health Risks
Respiratory issues, skin irritation
Storage and Disposal
Follow proper protocols
Safety Precautions
Handle with caution
Check Digit Verification of cas no
The CAS Registry Mumber 141535-83-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,5,3 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 141535-83:
(8*1)+(7*4)+(6*1)+(5*5)+(4*3)+(3*5)+(2*8)+(1*3)=113
113 % 10 = 3
So 141535-83-3 is a valid CAS Registry Number.
141535-83-3Relevant academic research and scientific papers
Condensation du chloroforme avec des olefins fluorees en milieu basique
Nguyen, Thoai,Wakselman, Claude
, p. 241 - 248 (2007/10/02)
The condensation of CHCl3 with CF3CF=CF2 under phase-transfer catalysis leads mainly to CF3CFH-CF=CCl2 (1a).In the case of CF2=CFCl, a cyclopropane adduct 3b is obtained along with CHClF-CF=CCl2 (1b).The yields of adducts 1a,b or 3b are ca. 30percent.As the working conditions are simple and the starting materials are readily available, the method could provide an interesting route to some perhalogeno-cyclopropanes and short-chain hydro-halogeno alkenes.
