2-(tert-Butyl)-4-chlorophenol

95%

Reagent Code: #145065
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CAS Number 13395-85-2

science Other reagents with same CAS 13395-85-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 184.66 g/mol
Formula C₁₀H₁₃ClO
badge Registry Numbers
MDL Number MFCD16657845
thermostat Physical Properties
Boiling Point 239°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in the synthesis of agrochemicals and pharmaceuticals. It serves in the production of certain herbicides and fungicides due to its stable phenolic structure and substituent groups that enhance bioactivity. Also employed as a building block in organic reactions, particularly in the development of antioxidants and stabilizers for industrial applications. Its chloro and tert-butyl functionalities make it suitable for coupling reactions and modification into more complex molecules.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿600.00
100mg
10-20 days ฿1,300.00
250mg
10-20 days ฿3,000.00
5g
10-20 days ฿35,650.00
1g
10-20 days ฿8,980.00
2-(tert-Butyl)-4-chlorophenol
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Used primarily as an intermediate in the synthesis of agrochemicals and pharmaceuticals. It serves in the production of certain herbicides and fungicides due to its stable phenolic structure and substituent groups that enhance bioactivity. Also employed as a building block in organic reactions, particularly in the development of antioxidants and stabilizers for industrial applications. Its chloro and tert-butyl functionalities make it suitable for coupling reactions and modification into more complex mol

Used primarily as an intermediate in the synthesis of agrochemicals and pharmaceuticals. It serves in the production of certain herbicides and fungicides due to its stable phenolic structure and substituent groups that enhance bioactivity. Also employed as a building block in organic reactions, particularly in the development of antioxidants and stabilizers for industrial applications. Its chloro and tert-butyl functionalities make it suitable for coupling reactions and modification into more complex molecules.

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