what reaction that produce 3-chlorobutanol? explain the process
Answers
Chlorobutanol
Names
IUPAC name
1,1,1-Trichloro-2-methylpropan-2-ol
Other names
1,1,1-Trichloro-2-methyl-2-propanol; Chlorbutol; Chloreton; Chloretone; Chlortran; Trichloro-tert-butyl alcohol; 1,1,1-Trichloro-tert-butyl alcohol; 2-(Trichloromethyl)propan-2-ol, 1,1,1-trichloro-2-methyl-2-propanol; tert-Trichlorobutyl alcohol; Trichloro-tert-butanol; Trichlorisobutylalcohol; 2,2,2-Trichloro-1,1-dimethylethanol
Identifiers
CAS Number
57-15-8
3D model (JSmol)
Interactive image
ChEMBL
ChEMBL1439973
ChemSpider
13842993
ECHA InfoCard 100.000.288
EC Number 200-317-6
KEGG
D01942
PubChem CID
5977
UNII
HM4YQM8WRC
InChI[show]
SMILES[show]
Properties
Chemical formula
C4H7Cl3O
Molar mass 177.45 g·mol−1
Appearance White solid
Odor Menthol
Melting point 95–99 °C (203–210 °F; 368–372 K)
Boiling point 167 °C (333 °F; 440 K)
Solubility in water
Slightly soluble
Solubility in acetone Soluble
Pharmacology
ATC code
A04AD04 (WHO)
Hazards
Main hazards Xn
NFPA 704
120
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references
Chlorobutanol (trichloro-2-methyl-2-propanol) is a preservative, sedative, hypnotic and weak local anesthetic similar in nature to chloral hydrate. It has antibacterial and antifungal properties. Chlorobutanol is typically used at a concentration of 0.5% where it lends long term stability to multi-ingredient formulations. However, it retains antimicrobial activity at 0.05% in water. Chlorobutanol has been used in anesthesia and euthanasia of invertebrates and fishes.[1][2] It is a white, volatile solid with a menthol-like odor.