2-(3-methoxyphenyl)-2-methylpropan-1-ol

95%

Reagent Code: #209310
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CAS Number 17653-95-1

science Other reagents with same CAS 17653-95-1

blur_circular Chemical Specifications

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Weight 180.12 g/mol
Formula C₁₁H₁₆O₂
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs). It serves as a building block in organic synthesis. Also applied in the preparation of fragrances and flavoring agents due to its aromatic characteristics. Its structural features, including the methoxy-substituted phenyl ring and primary alcohol group, make it valuable in the design of novel organic compounds for medicinal chemistry research. The methoxy and alcohol functionalities enable various transformations such as substitution, oxidation, or carbon-carbon bond formation, suitable for modifying molecular structures in drug development.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿3,168.00
inventory 1g
10-20 days ฿8,640.00
inventory 5g
10-20 days ฿30,600.00

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2-(3-methoxyphenyl)-2-methylpropan-1-ol
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs). It serves as a building block in organic synthesis. Also applied in the preparation of fragrances and flavoring agents due to its aromatic characteristics. Its structural features, including the methoxy-substituted phenyl ring and primary alcohol group, make it valuable in the design of novel organic compounds for medicinal chemistry research. The methoxy and alco

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs). It serves as a building block in organic synthesis. Also applied in the preparation of fragrances and flavoring agents due to its aromatic characteristics. Its structural features, including the methoxy-substituted phenyl ring and primary alcohol group, make it valuable in the design of novel organic compounds for medicinal chemistry research. The methoxy and alcohol functionalities enable various transformations such as substitution, oxidation, or carbon-carbon bond formation, suitable for modifying molecular structures in drug development.

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