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1-Chloro-3-methyl-2-butene

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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
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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
Flash point:
56 °F
storage temp. 
2-8°C
solubility 
soluble in Chloroform, Ethyl Acetate
form 
clear liquid
color 
Colorless to Light yellow
Water Solubility 
Miscible with chloroform, acetone, diethyl ether and alcohol. Immiscible with water.
CAS DataBase Reference
503-60-6(CAS DataBase Reference)
NIST Chemistry Reference
2-Butene, 1-chloro-3-methyl-(503-60-6)
EPA Substance Registry System
2-Butene, 1-chloro-3-methyl- (503-60-6)
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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 Data
503-60-6(Hazardous Substances Data)

MSDS

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1-Chloro-3-methyl-2-butene Usage And Synthesis

Chemical Properties

Colorless Liquid

Uses

1-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 Description

Kinetics 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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