(1-(2-Chlorophenyl)cyclobutyl)methanamine

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Reagent Code: #130919
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CAS Number 1227418-18-9

science Other reagents with same CAS 1227418-18-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 195.69 g/mol
Formula C₁₁H₁₄ClN
badge Registry Numbers
MDL Number MFCD16169400
thermostat Physical Properties
Boiling Point 292.7±23.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.149±0.06 g/cm3(Predicted)
Storage Room temperature, light-proof, inert gas

description Product Description

Used primarily as a research chemical in organic synthesis, particularly in the development of pharmaceutical intermediates. Its amine and cyclobutyl functional groups make it valuable for constructing complex molecules, especially in medicinal chemistry for exploring new bioactive compounds. The presence of a chlorine-substituted phenyl ring allows for further cross-coupling reactions, enabling the creation of diverse chemical libraries for drug discovery. It may also serve as a building block in the synthesis of central nervous system agents, though it is not used clinically. Handling requires caution due to potential reactivity and toxicity common to aromatic amines and chlorinated compounds.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿25,080.00
inventory 100mg
10-20 days ฿75,160.00

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(1-(2-Chlorophenyl)cyclobutyl)methanamine
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Used primarily as a research chemical in organic synthesis, particularly in the development of pharmaceutical intermediates. Its amine and cyclobutyl functional groups make it valuable for constructing complex molecules, especially in medicinal chemistry for exploring new bioactive compounds. The presence of a chlorine-substituted phenyl ring allows for further cross-coupling reactions, enabling the creation of diverse chemical libraries for drug discovery. It may also serve as a building block in the sy

Used primarily as a research chemical in organic synthesis, particularly in the development of pharmaceutical intermediates. Its amine and cyclobutyl functional groups make it valuable for constructing complex molecules, especially in medicinal chemistry for exploring new bioactive compounds. The presence of a chlorine-substituted phenyl ring allows for further cross-coupling reactions, enabling the creation of diverse chemical libraries for drug discovery. It may also serve as a building block in the synthesis of central nervous system agents, though it is not used clinically. Handling requires caution due to potential reactivity and toxicity common to aromatic amines and chlorinated compounds.

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