11-(2-Chloroacetyl)-5,11-dihydro-pyrido-[2,3-b][1,4]benzodiazepin-6-one

98%

Reagent Code: #159871
fingerprint
CAS Number 28797-48-0

science Other reagents with same CAS 28797-48-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 289.72 g/mol
Formula C₁₄H₁₂ClN₃O₂
badge Registry Numbers
MDL Number MFCD21648226
thermostat Physical Properties
Boiling Point 481.1ºC at 760 mmHg
inventory_2 Storage & Handling
Density 1.415
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of certain pharmaceutical compounds, particularly in the development of benzodiazepine derivatives with potential central nervous system activity. It serves as a key building block for creating compounds that may exhibit anxiolytic, anticonvulsant, or sedative properties. Its reactive chloroacetyl group allows for further chemical modifications, enabling the attachment of various functional groups to fine-tune biological activity. Primarily utilized in research settings for drug discovery and development.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿390.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
11-(2-Chloroacetyl)-5,11-dihydro-pyrido-[2,3-b][1,4]benzodiazepin-6-one
No image available

Used as an intermediate in the synthesis of certain pharmaceutical compounds, particularly in the development of benzodiazepine derivatives with potential central nervous system activity. It serves as a key building block for creating compounds that may exhibit anxiolytic, anticonvulsant, or sedative properties. Its reactive chloroacetyl group allows for further chemical modifications, enabling the attachment of various functional groups to fine-tune biological activity. Primarily utilized in research se

Used as an intermediate in the synthesis of certain pharmaceutical compounds, particularly in the development of benzodiazepine derivatives with potential central nervous system activity. It serves as a key building block for creating compounds that may exhibit anxiolytic, anticonvulsant, or sedative properties. Its reactive chloroacetyl group allows for further chemical modifications, enabling the attachment of various functional groups to fine-tune biological activity. Primarily utilized in research settings for drug discovery and development.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...