10124-73-9 Usage
Chemical Family
Chloro alkenes
1-Hexene, 2-chlorobelongs to the family of chloro alkenes, which are organic compounds containing a carbon-chlorine bond and a carbon-carbon double bond.
Structure
Six-carbon chain with a double bond and a chlorine atom
The compound has a six-carbon chain with a carbon-carbon double bond, and a chlorine atom is attached to the second carbon atom.
Physical State
Clear, colorless liquid
1-Hexene, 2-chlorois a clear, colorless liquid, which is a common physical state for many organic compounds.
Odor
Mild, sweet
The compound has a mild, sweet odor, which may be detectable at certain concentrations.
Uses
Production of epoxides, glycols, and polymers
1-Hexene, 2-chlorois primarily used in the production of various chemical compounds, such as epoxides, glycols, and polymers, making it an important intermediate in the synthesis of other compounds.
Application
Intermediate in synthesis
The main application of 1-Hexene, 2-chlorois as an intermediate in the synthesis of other compounds, rather than being directly used in consumer products or industrial applications.
Health Hazards
Potential health risks
It is important to handle 1-Hexene, 2-chlorowith caution, as it may pose health hazards if not properly managed. This includes taking appropriate safety measures to avoid exposure and following proper storage and disposal guidelines.
Check Digit Verification of cas no
The CAS Registry Mumber 10124-73-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,2 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 10124-73:
(7*1)+(6*0)+(5*1)+(4*2)+(3*4)+(2*7)+(1*3)=49
49 % 10 = 9
So 10124-73-9 is a valid CAS Registry Number.
10124-73-9Relevant academic research and scientific papers
FeCl3-H2O: A specific system for arylacetylene hydration
Damiano, Jean Pierre,Postel, Michele
, p. 303 - 305 (2007/10/03)
FeCl3 has been found to be very specifically effective in the hydration of terminal aromatic alkynes to the corresponding methylketones.
