Names | |
---|---|
Preferred IUPAC name
1,1,1,2,2,3,3-Heptachloropropane | |
Identifiers | |
3D model (
JSmol)
|
|
ChemSpider | |
ECHA InfoCard | 100.008.962 |
EC Number |
|
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C3HCl7 | |
Molar mass | 285.21 g/mol |
Melting point | 29 °C (84 °F; 302 K) |
Boiling point | 243.5 °C (470.3 °F; 516.6 K) |
Hazards | |
GHS labelling: | |
Warning | |
H315, H319, H335, H413 | |
P261, P264, P271, P273, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501 | |
Related compounds | |
Related compounds
|
1,1,1,2,3,3,3-Heptafluoropropane |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
1,1,1,2,2,3,3-Heptachloropropane is a compound of chlorine, hydrogen, and carbon. [1] Its linear formula is C2Cl5CHCl2. [2]
Heptachloropropane is made in a modified Friedel-Crafts or Prins reaction from chloroform and tetrachloroethylene with catalytic aluminum chloride. Dehydrochlorination with a base gives hexachloropropene. [3]
Names | |
---|---|
Preferred IUPAC name
1,1,1,2,2,3,3-Heptachloropropane | |
Identifiers | |
3D model (
JSmol)
|
|
ChemSpider | |
ECHA InfoCard | 100.008.962 |
EC Number |
|
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C3HCl7 | |
Molar mass | 285.21 g/mol |
Melting point | 29 °C (84 °F; 302 K) |
Boiling point | 243.5 °C (470.3 °F; 516.6 K) |
Hazards | |
GHS labelling: | |
Warning | |
H315, H319, H335, H413 | |
P261, P264, P271, P273, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501 | |
Related compounds | |
Related compounds
|
1,1,1,2,3,3,3-Heptafluoropropane |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
1,1,1,2,2,3,3-Heptachloropropane is a compound of chlorine, hydrogen, and carbon. [1] Its linear formula is C2Cl5CHCl2. [2]
Heptachloropropane is made in a modified Friedel-Crafts or Prins reaction from chloroform and tetrachloroethylene with catalytic aluminum chloride. Dehydrochlorination with a base gives hexachloropropene. [3]