7-Hydroxy-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid

98%

Reagent Code: #197035
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CAS Number 31846-36-3

science Other reagents with same CAS 31846-36-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 192.21 g/mol
Formula C₁₁H₁₂O₃
badge Registry Numbers
MDL Number MFCD08061210
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system (CNS) active compounds. Its structural features make it valuable in medicinal chemistry for building rigid, conformationally restricted scaffolds that enhance binding affinity and metabolic stability. It is also employed in the preparation of enzyme inhibitors and receptor modulators, especially targeting neurological and psychiatric disorders. Additionally, it serves as a chiral building block in asymmetric synthesis, enabling the production of enantiomerically pure drugs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,260.00
inventory 250mg
10-20 days ฿3,010.00

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7-Hydroxy-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system (CNS) active compounds. Its structural features make it valuable in medicinal chemistry for building rigid, conformationally restricted scaffolds that enhance binding affinity and metabolic stability. It is also employed in the preparation of enzyme inhibitors and receptor modulators, especially targeting neurological and

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system (CNS) active compounds. Its structural features make it valuable in medicinal chemistry for building rigid, conformationally restricted scaffolds that enhance binding affinity and metabolic stability. It is also employed in the preparation of enzyme inhibitors and receptor modulators, especially targeting neurological and psychiatric disorders. Additionally, it serves as a chiral building block in asymmetric synthesis, enabling the production of enantiomerically pure drugs.

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