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Home > Encyclopedia > 1-Chloro-4-(1-methylethenyl)benzene

1-Chloro-4-(1-methylethenyl)benzene

1-Chloro-4-(1-methylethenyl)benzene structure

1-Chloro-4-(1-methylethenyl)benzene 

structure
  • CAS No:

    1712-70-5

  • Formula:

    C9H9Cl

  • Chemical Name:

    1-Chloro-4-(1-methylethenyl)benzene

  • Synonyms:

    Benzene,1-chloro-4-(1-methylethenyl)-;Styrene,p-chloro-α-methyl-;1-Chloro-4-(1-methylethenyl)benzene;p-Chloro-α-methylstyrene;4-Chloro-α-methylstyrene;2-(p-Chlorophenyl)propene;2-(4-Chlorophenyl)propene;1-Chloro-4-isopropenylbenzene;p-Chloroisopropenylbenzene;α-Methyl-p-chlorostyrene;2-(4-Chlorophenyl)-1-propene;α-Methyl-4-chlorostyrene;4-Isopropenylphenyl chloride;1-Chloro-4-(prop-1-en-2-yl)benzene;4-Isopropenyl-1-chlorobenzene

  • Categories:

    Chemical Reagents  >  Organic Reagents

Description

clear colorless to pale yellow liquid

1-Chloro-4-(1-methylethenyl)benzene Basic Attributes

152.62

152.62

1855073

216-984-1

DTXSID40169024

29036990

Characteristics

0

3.78

1.0750 g/cm3 @ Temp: 20 °C

3.5ºC

89 °C

165 °F

n 20/D 1.555(lit.)

Soluble in water.

0-6°C

Safety Information

III

9

3082

3

23-24/25

P261, P264, P271, P273, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P391, P403+P233, P405, P501

H315

|Warning|H315 (80%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P273, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P391, P403+P233, P405, and P501|Aggregated GHS information provided by 5 companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Toxicity

691.83

Drug Information

19.95 Days

1-Chloro-4-(1-methylethenyl)benzene Use and Manufacturing

Methods of Manufacturing

It is obtained by addition, hydrolysis and elimination of p-dichlorobenzene. 1. Addition and hydrolysis Add magnesium chips and tetrahydrofuran into the reaction pot and stir and heat, and add initiator methyl iodide at 60°C. When the fierce reaction started, a mixture of p-dichlorobenzene and tetrahydrofuran was added and refluxed for 2h. Cool to 15°C, slowly add acetone, stir and let stand overnight. Then add ammonium chloride ice water and concentrated hydrochloric acid to hydrolyze below 20°C. The oil layer is washed with sulfuric acid, then washed with water to neutrality, dried with anhydrous calcium chloride, filtered to remove the desiccant, and distilled under reduced pressure to obtain p-chlorobenzene dimethyl methanol. 2. Elimination Put the crushed potassium hydrogen sulfate into a reaction pot with a fractionating column, heat it to 210-220°C, melt, and add p-chlorobenzene dimethyl methanol dropwise under reduced pressure. Collect the distillate at 120-140℃ (5.33-6.67kPa), re-steam it again, and collect the distillate at 80-90℃ (2.0kPa) to obtain the finished product.

Uses

Organic intermediates.

Computed Properties

Molecular Weight:152.62
XLogP3:4.4
Rotatable Bond Count:1
Exact Mass:152.0392780
Monoisotopic Mass:152.0392780
Heavy Atom Count:10
Complexity:121
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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