1,3,5-Tri-tert-butylbenzene

98%

Reagent Code: #239842
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Alias 1,3,5-Tri-tert-butylbenzene
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CAS Number 1460-02-2

science Other reagents with same CAS 1460-02-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 246.43 g/mol
Formula C₁₈H₃₀
badge Registry Numbers
EC Number 215-952-4
MDL Number MFCD00008831
thermostat Physical Properties
Melting Point 67-72 °C(lit.)
Boiling Point 121-122 °C12 mm Hg(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a sterically hindered aromatic compound in organic synthesis, particularly in the development of catalysts and ligands for transition metal complexes. Its bulky tert-butyl groups provide strong electron-donating effects and prevent unwanted side reactions by shielding the aromatic ring, making it valuable in stabilizing reactive intermediates. Commonly employed in the study of reaction mechanisms and in the design of advanced materials where controlled molecular geometry is essential. Also finds use in the synthesis of dendrimers and other highly branched macromolecules due to its rigid, symmetrical structure.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿300.00
inventory 25g
10-20 days ฿650.00
inventory 100g
10-20 days ฿2,430.00
inventory 500g
10-20 days ฿9,380.00

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1,3,5-Tri-tert-butylbenzene
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Used as a sterically hindered aromatic compound in organic synthesis, particularly in the development of catalysts and ligands for transition metal complexes. Its bulky tert-butyl groups provide strong electron-donating effects and prevent unwanted side reactions by shielding the aromatic ring, making it valuable in stabilizing reactive intermediates. Commonly employed in the study of reaction mechanisms and in the design of advanced materials where controlled molecular geometry is essential. Also finds

Used as a sterically hindered aromatic compound in organic synthesis, particularly in the development of catalysts and ligands for transition metal complexes. Its bulky tert-butyl groups provide strong electron-donating effects and prevent unwanted side reactions by shielding the aromatic ring, making it valuable in stabilizing reactive intermediates. Commonly employed in the study of reaction mechanisms and in the design of advanced materials where controlled molecular geometry is essential. Also finds use in the synthesis of dendrimers and other highly branched macromolecules due to its rigid, symmetrical structure.

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