[4-(3,5-Dichlorophenyl)phenyl]methylamine hydrochloride

95%

Reagent Code: #178310
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CAS Number 518357-39-6

science Other reagents with same CAS 518357-39-6

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inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of selective receptor modulators. Its structure supports the creation of bioactive molecules with potential activity in central nervous system disorders. It is also employed in the preparation of agrochemicals and specialty polymers where aromatic amine functionality is required. Due to the presence of both aryl chloride and amine groups, it serves as a versatile building block in cross-coupling and nucleophilic substitution reactions in medicinal chemistry research.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿4,800.00
250mg
10-20 days ฿8,000.00
500mg
10-20 days ฿14,080.00
1g
10-20 days ฿22,400.00
5g
10-20 days ฿78,400.00
[4-(3,5-Dichlorophenyl)phenyl]methylamine hydrochloride
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Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of selective receptor modulators. Its structure supports the creation of bioactive molecules with potential activity in central nervous system disorders. It is also employed in the preparation of agrochemicals and specialty polymers where aromatic amine functionality is required. Due to the presence of both aryl chloride and amine groups, it serves as a versatile building block in cross-coup

Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of selective receptor modulators. Its structure supports the creation of bioactive molecules with potential activity in central nervous system disorders. It is also employed in the preparation of agrochemicals and specialty polymers where aromatic amine functionality is required. Due to the presence of both aryl chloride and amine groups, it serves as a versatile building block in cross-coupling and nucleophilic substitution reactions in medicinal chemistry research.

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