2-(2-Bromo-6-chlorophenyl)acetonitrile

95%

Reagent Code: #153522
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CAS Number 76574-39-5

science Other reagents with same CAS 76574-39-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.5 g/mol
Formula C₈H₅BrClN
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MDL Number MFCD15526749
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of angiotensin II receptor antagonists like valsartan and related sartan-class drugs. It plays a key role in constructing the core structure of these antihypertensive agents. The nitrile and halogen groups allow further functionalization, enabling coupling reactions and ring formation essential in active pharmaceutical ingredient (API) manufacturing. Commonly employed in multi-step organic synthesis under controlled conditions due to its reactivity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,720.00
inventory 1g
10-20 days ฿5,340.00
inventory 5g
10-20 days ฿20,650.00

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2-(2-Bromo-6-chlorophenyl)acetonitrile
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of angiotensin II receptor antagonists like valsartan and related sartan-class drugs. It plays a key role in constructing the core structure of these antihypertensive agents. The nitrile and halogen groups allow further functionalization, enabling coupling reactions and ring formation essential in active pharmaceutical ingredient (API) manufacturing. Commonly employed in multi-step organic synthesis under controll

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of angiotensin II receptor antagonists like valsartan and related sartan-class drugs. It plays a key role in constructing the core structure of these antihypertensive agents. The nitrile and halogen groups allow further functionalization, enabling coupling reactions and ring formation essential in active pharmaceutical ingredient (API) manufacturing. Commonly employed in multi-step organic synthesis under controlled conditions due to its reactivity.

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