N-(5-Aminopentyl)acetamide hydrochloride

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Reagent Code: #218052
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Alias Related CAS number: 32343-73-0
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CAS Number 102029-76-5

science Other reagents with same CAS 102029-76-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.68 g/mol
Formula C₇H₁₇ClN₂O
badge Registry Numbers
MDL Number MFCD00058001
thermostat Physical Properties
Boiling Point 110°C/0.02mmHg(lit.)
inventory_2 Storage & Handling
Density 0.98g/ml
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of bioactive molecules and pharmaceuticals. It serves as a building block for the development of amine-containing compounds, including enzyme inhibitors and receptor ligands. Its structure supports conjugation in peptide-like frameworks, making it valuable in medicinal chemistry for drug design and optimization. Also utilized in the synthesis of certain fluorescent probes and labeling agents due to its amine functionality after deprotection.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿2,980.00
5g
10-20 days ฿12,850.00
N-(5-Aminopentyl)acetamide hydrochloride
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Used as an intermediate in organic synthesis, particularly in the preparation of bioactive molecules and pharmaceuticals. It serves as a building block for the development of amine-containing compounds, including enzyme inhibitors and receptor ligands. Its structure supports conjugation in peptide-like frameworks, making it valuable in medicinal chemistry for drug design and optimization. Also utilized in the synthesis of certain fluorescent probes and labeling agents due to its amine functionality after

Used as an intermediate in organic synthesis, particularly in the preparation of bioactive molecules and pharmaceuticals. It serves as a building block for the development of amine-containing compounds, including enzyme inhibitors and receptor ligands. Its structure supports conjugation in peptide-like frameworks, making it valuable in medicinal chemistry for drug design and optimization. Also utilized in the synthesis of certain fluorescent probes and labeling agents due to its amine functionality after deprotection.

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