2-Amino-5-chlorobenzophenone

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Reagent Code: #134521
label
Alias 2-amino-5-chlorobenzophenone
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CAS Number 719-59-5

science Other reagents with same CAS 719-59-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.68 g/mol
Formula C₁₃H₁₀ClNO
badge Registry Numbers
EC Number 211-949-7
MDL Number MFCD00007839
thermostat Physical Properties
Melting Point 96-98 °C(lit.)
Boiling Point 207 °C
inventory_2 Storage & Handling
Density 1.33
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of certain benzodiazepine derivatives which are important in anxiolytic and sedative drugs. It also serves as a building block in the development of organic compounds for photoinitiators and UV absorbers used in coatings and polymers. Its structure allows for further functionalization, making it valuable in research and development of new bioactive molecules.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿300.00
inventory 100g
10-20 days ฿620.00
inventory 500g
10-20 days ฿2,650.00
inventory 2.5kg
10-20 days ฿13,140.00
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2-Amino-5-chlorobenzophenone
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of certain benzodiazepine derivatives which are important in anxiolytic and sedative drugs. It also serves as a building block in the development of organic compounds for photoinitiators and UV absorbers used in coatings and polymers. Its structure allows for further functionalization, making it valuable in research and development of new bioactive molecules.

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of certain benzodiazepine derivatives which are important in anxiolytic and sedative drugs. It also serves as a building block in the development of organic compounds for photoinitiators and UV absorbers used in coatings and polymers. Its structure allows for further functionalization, making it valuable in research and development of new bioactive molecules.

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