N-[4-[(7-Chloro-2,3,4,5-tetrahydro-5-oxo-1H-1-benzazepin-1-yl)carbonyl]-3-methylphenyl]-2-methylbenzamide

99%

Reagent Code: #216957
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CAS Number 137973-76-3

science Other reagents with same CAS 137973-76-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 446.92 g/mol
Formula C₂₆H₂₃ClN₂O₃
thermostat Physical Properties
Boiling Point 593.2±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.307g/cm3
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of anti-inflammatory and analgesic agents. Its structure supports binding to specific enzyme targets involved in pain and inflammation pathways. Commonly employed in research settings for optimizing drug candidates with improved efficacy and reduced side effects. Also utilized in the preparation of analogs for structure-activity relationship (SAR) studies in medicinal chemistry.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿3,450.00
1g
10-20 days ฿6,960.00
25g
10-20 days ฿71,100.00
5g
10-20 days ฿18,150.00
N-[4-[(7-Chloro-2,3,4,5-tetrahydro-5-oxo-1H-1-benzazepin-1-yl)carbonyl]-3-methylphenyl]-2-methylbenzamide
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of anti-inflammatory and analgesic agents. Its structure supports binding to specific enzyme targets involved in pain and inflammation pathways. Commonly employed in research settings for optimizing drug candidates with improved efficacy and reduced side effects. Also utilized in the preparation of analogs for structure-activity relationship (SAR) studies in medicinal chemistry.

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of anti-inflammatory and analgesic agents. Its structure supports binding to specific enzyme targets involved in pain and inflammation pathways. Commonly employed in research settings for optimizing drug candidates with improved efficacy and reduced side effects. Also utilized in the preparation of analogs for structure-activity relationship (SAR) studies in medicinal chemistry.

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