3-(Aminomethyl)-5-methylhexanoic acid

98%

Reagent Code: #137416
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CAS Number 130912-52-6

science Other reagents with same CAS 130912-52-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 159.23 g/mol
Formula C₈H₁₇NO₂
thermostat Physical Properties
Boiling Point 274 °C at 760 mmHg (lit.)
inventory_2 Storage & Handling
Density 0.997 g/cm3 at 25 °C (lit.)
Storage Room temperature

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. It serves as a building block for gamma-aminobutyric acid (GABA) analogs, which are important in the treatment of neurological disorders such as epilepsy, neuropathic pain, and anxiety. Its structural features allow for modification to enhance blood-brain barrier penetration and receptor specificity. Also employed in research settings for exploring new bioactive molecules and structure-activity relationships in neuropharmacology.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,900.00
inventory 5g
10-20 days ฿13,500.00
inventory 25g
10-20 days ฿48,000.00

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3-(Aminomethyl)-5-methylhexanoic acid
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Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. It serves as a building block for gamma-aminobutyric acid (GABA) analogs, which are important in the treatment of neurological disorders such as epilepsy, neuropathic pain, and anxiety. Its structural features allow for modification to enhance blood-brain barrier penetration and receptor specificity. Also employed in research settings for exploring new bioactive molecul

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. It serves as a building block for gamma-aminobutyric acid (GABA) analogs, which are important in the treatment of neurological disorders such as epilepsy, neuropathic pain, and anxiety. Its structural features allow for modification to enhance blood-brain barrier penetration and receptor specificity. Also employed in research settings for exploring new bioactive molecules and structure-activity relationships in neuropharmacology.

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