(/-)-1-METHOXY-1-(TRIFLUOROMETHYL)PHENYLACETYL CHLORIDE

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Reagent Code: #113883
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CAS Number 64312-89-6

science Other reagents with same CAS 64312-89-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.62 g/mol
Formula C₁₀H₈ClF₃O₂
badge Registry Numbers
MDL Number MFCD00078209
thermostat Physical Properties
Boiling Point 213-214 °C(lit.)
inventory_2 Storage & Handling
Density 1.327 g/mL at 25 °C(lit.)
Storage 2-8°C, sealed, dry, inflated

description Product Description

This specialty chemical is an acyl chloride derivative of methoxy(trifluoromethyl)phenylacetic acid, commonly known as Mosher's acid chloride. It is primarily used as a chiral derivatizing agent in organic chemistry for the preparation of Mosher's esters, which enable the determination of enantiomeric purity and absolute configuration via NMR spectroscopy. This makes it invaluable in pharmaceutical research for analyzing chiral compounds and developing enantiomerically pure APIs. Additionally, its reactive acyl chloride group allows it to serve as a versatile building block in the synthesis of amides, esters, and other derivatives for more complex molecules in agrochemicals, where the trifluoromethyl group enhances biological activity and metabolic stability. It also finds applications in materials science for modifying polymers and creating functionalized coatings with tailored properties. As a key intermediate, its niche reactivity supports advanced research and industrial processes in stereochemistry and fine chemical synthesis.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,168.00
inventory 250mg
10-20 days ฿2,151.00
inventory 5g
10-20 days ฿13,437.00

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(/-)-1-METHOXY-1-(TRIFLUOROMETHYL)PHENYLACETYL CHLORIDE
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This specialty chemical is an acyl chloride derivative of methoxy(trifluoromethyl)phenylacetic acid, commonly known as Mosher's acid chloride. It is primarily used as a chiral derivatizing agent in organic chemistry for the preparation of Mosher's esters, which enable the determination of enantiomeric purity and absolute configuration via NMR spectroscopy. This makes it invaluable in pharmaceutical research for analyzing chiral compounds and developing enantiomerically pure APIs. Additionally, its reacti

This specialty chemical is an acyl chloride derivative of methoxy(trifluoromethyl)phenylacetic acid, commonly known as Mosher's acid chloride. It is primarily used as a chiral derivatizing agent in organic chemistry for the preparation of Mosher's esters, which enable the determination of enantiomeric purity and absolute configuration via NMR spectroscopy. This makes it invaluable in pharmaceutical research for analyzing chiral compounds and developing enantiomerically pure APIs. Additionally, its reactive acyl chloride group allows it to serve as a versatile building block in the synthesis of amides, esters, and other derivatives for more complex molecules in agrochemicals, where the trifluoromethyl group enhances biological activity and metabolic stability. It also finds applications in materials science for modifying polymers and creating functionalized coatings with tailored properties. As a key intermediate, its niche reactivity supports advanced research and industrial processes in stereochemistry and fine chemical synthesis.

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