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620-72-4 - Phenyl bromoacetate, 98% - Bromoacetic acid phenyl ester - H60464 - Alfa Aesar

H60464 Phenyl bromoacetate, 98%

CAS Number
620-72-4
Synonyms
Bromoacetic acid phenyl ester

Size Price ($) Quantity Availability
5g 25.75
50g 209.09
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Phenyl bromoacetate, 98%

MDL
MFCD00192391

Chemical Properties

Formula
C8H7BrO2
Formula Weight
215.04
Melting point
31-33°
Boiling Point
134°
Flash Point
113°(235°F)
Density
1.508
Solubility
Soluble in ethanol and ether, insoluble in water.

Applications

Phenyl bromoacetate may be employed as alkylation reagent in the preparation of 2-(phenoxycarbonyl)methyl triazoles. It may be used in the synthesis of the A-ring of cylindrospermopsin and in the synthesis of 2-{2-[1-(4-hydroxy-6-methyl-2-oxo-2H-pyran-3-yl)ethylidene]hydrazinyl}-1,3-thiazolidin-4-one3, 2-{2-[1-(4-hydroxy-6-methyl-2-oxo-2H-pyran-3-yl)ethylidene]hydrazinyl}-3-methyl-1,3-thiazolidin-4-one3, 3-ethyl-2-{2-[1-(4-hydroxy-6-methyl-2-oxo-2H-pyran-3-yl)ethylidene]hydrazinyl}-1,3-thiazolidin-4-one3 and 2-{2-[1-(4-hydroxy-6-methyl-2-oxo-2H-pyran-3-yl)ethylidene] hydrazinyl}-3-phenyl-1,3-thiazolidin-4-one3.

Notes

Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store under inert gas.

Literature References

Reynold C. Fuson.; Norman. Thomas. Extension of the Reformatsky Reaction to new Types of Compounds. J. Org. Chem. 1953, 18 (12),1762-1766.

Hans Thacher Clarke. XLVI.—The relation between reactivity and chemical constitution of certain halogen compounds. J. Chem. Soc., Trans. 1910, 97 416-429.

Other References

Harmonized Tariff Code
2915.90
TSCA
No

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