2,2-Difluoropropane-1,3-Diamine Dihydrochloride

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Reagent Code: #177396
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CAS Number 133186-53-5

science Other reagents with same CAS 133186-53-5

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Weight 183.03 g/mol
Formula C₃H₁₀Cl₂F₂N₂
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MDL Number MFCD23378436
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure supports the creation of complex organic molecules by serving as a building block with enhanced bioavailability and metabolic stability. Commonly employed in medicinal chemistry for constructing nitrogen-containing heterocycles and functionalized amines. Also utilized in the preparation of novel kinase inhibitors and protease inhibitors due to its favorable reactivity and compatibility with various coupling reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,640.00
inventory 250mg
10-20 days ฿11,250.00
inventory 1g
10-20 days ฿30,340.00

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2,2-Difluoropropane-1,3-Diamine Dihydrochloride
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure supports the creation of complex organic molecules by serving as a building block with enhanced bioavailability and metabolic stability. Commonly employed in medicinal chemistry for constructing nitrogen-containing heterocycles and functionalized amines. Also utilized in the preparation of novel kinase inhibitors and protease inhibitors due to its favorable rea

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure supports the creation of complex organic molecules by serving as a building block with enhanced bioavailability and metabolic stability. Commonly employed in medicinal chemistry for constructing nitrogen-containing heterocycles and functionalized amines. Also utilized in the preparation of novel kinase inhibitors and protease inhibitors due to its favorable reactivity and compatibility with various coupling reactions.

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