1-Chloro-3-methyl-2-butene

1-Chloro-3-methyl-2-butene
  • CAS No.:503-60-6
Other grades of this product :
1-Chloro-3-methyl-2-butene Basic information
Product Name:1-Chloro-3-methyl-2-butene
Synonyms:1-Chloro-3-methyl-2-butene,95%,stab.withpotassiumcarbonate;1-CHLORO-3-METHYL-2-BUTENE , STABILIZED WITH POTASSIUM CARBONATE;1-CHLORO-3-METHYL-2-BUTENE 96+%;1-Chloro-3-methyl-2-butene (stabilized with K2CO3);Isopentenyl chloride;1-Chloro-3-methyl-2-;3,3-Dimethylallyl chloride, Prenyl chloride;1-Chloro-3-methyl-2-butene,95% (99% min. total isomers)
CAS:503-60-6
MF:C5H9Cl
MW:104.58
EINECS:207-972-7
Product Categories:API Intermediate;Alkenyl;Halogenated Hydrocarbons;Organic Building Blocks
Mol File:503-60-6.mol
1-Chloro-3-methyl-2-butene Chemical Properties
Boiling point 58-59 °C/120 mmHg (lit.)
density 0.928 g/mL at 25 °C (lit.)
refractive index n20/D 1.4488(lit.)
RTECS EM4298500
Fp 56 °F
storage temp. 2-8°C
form clear liquid
color Colorless to Light yellow
Water Solubility Miscible with chloroform, acetone, diethyl ether and alcohol. Immiscible with water.
CAS DataBase Reference503-60-6(CAS DataBase Reference)
NIST Chemistry Reference2-Butene, 1-chloro-3-methyl-(503-60-6)
EPA Substance Registry System2-Butene, 1-chloro-3-methyl- (503-60-6)
Safety Information
Hazard Codes F,Xi
Risk Statements 11-36/37/38
Safety Statements 16-26-27-36/37/39
RIDADR UN 1993 3/PG 2
WGK Germany 3
TSCA Yes
HazardClass 3
PackingGroup III
HS Code 29032990
Hazardous Substances Data503-60-6(Hazardous Substances Data)
MSDS Information
ProviderLanguage
1-Chloro-3-methyl-2-butene English
SigmaAldrich English
ALFA English
1-Chloro-3-methyl-2-butene Usage And Synthesis
Chemical PropertiesColorless Liquid
Uses1-Chloro-3-methyl-2-butene is used in the synthesis of geraniol. It is also used as an alkylating agent and as a reagent in hyperforin. Further, it is used as an antibiotic to inhibit growth of tumor cells.
General DescriptionKinetics of gas-phase reactions of ozone with 1-chloro-3-methyl-2-butene was studied. Reaction of 1-chloro-3-methyl-2-butene with potassium iodide in acetone and sodium ethoxide in ethanol was studied.

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