2-Bromo-1-phenylpropane
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2-Bromo-1-phenylpropane
structure -
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CAS No:
2114-39-8
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Formula:
C9H11Br
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Chemical Name:
2-Bromo-1-phenylpropane
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Synonyms:
Benzene,(2-bromopropyl)-;(2-Bromopropyl)benzene;1-Phenyl-2-bromopropane;2-Bromo-1-phenylpropane;1-Bromo-1-methyl-2-phenylethane;(±)-2-Bromo-1-phenylpropane;14367-52-3
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CAS No:
Description
This organic bromide consists of a phenyl group attached to a brominated propane chain. It serves as an intermediate in chemical synthesis.
This organic bromide consists of a phenyl group attached to a brominated propane chain. It serves as an intermediate in chemical synthesis.
Characteristics
0
3.01250
1.291 g/mL at 25 °C(lit.)
-10°C (estimate)
92-93 °C @ Press: 10 Torr
195 °F
n20/D 1.545(lit.)
Safety Information
NA 1993 / PGIII
3
36/37/38
26
Xi
P261-P305 + P351 + P338
H315-H319-H335
|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 39 companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
2-Bromo-1-phenylpropane Use and Manufacturing
2-Bromo-1-phenylpropane is an important organic synthetic intermediate, which can be used to synthesize various organic compounds. It can be used as an initiator, catalyst or additive in synthesis and research applications. It can be used to make trans-beta-methylstyrene. The common preparation of 2-Bromo-1-phenylpropane is by bromination. The specific step is to react phenylpropane with ozone to get benzaldehyde, benzyl alcohol and other reaction products, and then brominate benzyl alcohol with HBr solution to get 2-Bromo-1-phenylpropane.
2-Bromo-1-phenylpropane is an important organic synthetic intermediate, which can be used to synthesize various organic compounds. It can be used as an initiator, catalyst or additive in synthesis and research applications. It can be used to make trans-beta-methylstyrene. The common preparation of 2-Bromo-1-phenylpropane is by bromination. The specific step is to react phenylpropane with ozone to get benzaldehyde, benzyl alcohol and other reaction products, and then brominate benzyl alcohol with HBr solution to get 2-Bromo-1-phenylpropane.
Computed Properties
Molecular Weight:199.09
XLogP3:3.4
Rotatable Bond Count:2
Exact Mass:198.00441
Monoisotopic Mass:198.00441
Heavy Atom Count:10
Complexity:84.7
Undefined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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