110800-91-4 Usage
Physical state
Liquid
Color
Colorless
Flammability
Nonflammable
Molecular weight
202.9 g/mol
Boiling point
-3.4°C (27.3°F)
Melting point
-98°C (-143.4°F)
Density
1.52 g/cm3
Solubility
Soluble in nonpolar solvents
Volatile organic compound (VOC)
Yes
Uses
Intermediate in the production of refrigerants and propellants, solvent for cleaning and degreasing
Environmental impact
Potential to contribute to air pollution and ozone depletion
Safety regulations
Handle and use with care, in accordance with safety regulations to minimize impact on human health and the environment
Reactivity
May react with strong oxidizing agents, bases, and reducing agents
Storage
Store in a cool, dry, well-ventilated area, away from heat, sparks, and open flames
Disposal
Dispose of in accordance with local, national, and international regulations for hazardous materials
Personal protective equipment (PPE)
Wear appropriate PPE, such as gloves, goggles, and a respirator, when handling this chemical
Health hazards
Inhalation may cause respiratory irritation, and prolonged exposure may lead to headaches, dizziness, and nausea
First aid measures
In case of skin contact, wash with plenty of soap and water; in case of eye contact, rinse with plenty of water; if inhaled, move to fresh air and seek medical attention if necessary; if swallowed, do not induce vomiting and seek medical attention immediately.
Check Digit Verification of cas no
The CAS Registry Mumber 110800-91-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,8,0 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 110800-91:
(8*1)+(7*1)+(6*0)+(5*8)+(4*0)+(3*0)+(2*9)+(1*1)=74
74 % 10 = 4
So 110800-91-4 is a valid CAS Registry Number.
110800-91-4Relevant academic research and scientific papers
REACTIONS OF PERCHLOROFLUORO COMPOUNDS VI. REARRANGEMENT OF HIGHER PERCHLOROFLUOROOLEFINS AND THEIR REACTIONS WITH NUCLEOPHILES AND ELECTROPHILES
Chang-Ming Hu,Hui Liu,Ze-Qi Xu
, p. 491 - 506 (2007/10/02)
The fluoride ion induced isomerization of CFCl2CF2CFClCF2CF=CF2 (1) gave only trans isomer CFCl2CF2CFClCF=CFCF3 (2), then trans CFCl2CF2CCl=CFCF2CF3 (3) and trans CFCl2CF2CF=CFCF2CF3 (4), with the latter in predominance, while AlCl3-catalyzed isomerisation of 1 gave only 2 and 3.No cis isomer could be detected.Such isomerization was terminated once a chlorine atom was linked to the double bond.Reactions of perchlorofluoroolefins 1, 2 and 3 with various nucleophiles have been studied.With terminal olefin 1, C-1 was exclusively attacked by nucleophiles with the formation of three kinds of products.In 2, merely C-2 was attacked and as a chlorine atom was just located at the allylic position, the reaction only proceeded through a SN2' mechanism.In 3, only C-4 was attacked and no protonation product could be found.Competitive reaction showed the reactivity of these three perchlorofluoroolefins decreased in this order: 1 > 3 > 2, which was directly related to the polarity of double bond.Only 1 reacted with electrophiles under normal conditions.
