3,5-Bis(tert-butylthio)-1-chlorobenzene

98%

Reagent Code: #147683
fingerprint
CAS Number 260968-02-3

science Other reagents with same CAS 260968-02-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 288.89 g/mol
Formula C₁₄H₂₁ClS₂
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily as an intermediate in the synthesis of agrochemicals and pharmaceuticals, this compound serves as a building block for sulfur-containing organic molecules. Its chloro and tert-butylthio groups enable selective functionalization in cross-coupling reactions, making it valuable in the development of crop protection agents. It is also employed in research settings to design complex molecules requiring sterically hindered thioether motifs. The stability imparted by the tert-butyl groups enhances its utility in reaction pathways where decomposition is a concern.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿1,260.00
inventory 1g
10-20 days ฿2,930.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3,5-Bis(tert-butylthio)-1-chlorobenzene
No image available

Used primarily as an intermediate in the synthesis of agrochemicals and pharmaceuticals, this compound serves as a building block for sulfur-containing organic molecules. Its chloro and tert-butylthio groups enable selective functionalization in cross-coupling reactions, making it valuable in the development of crop protection agents. It is also employed in research settings to design complex molecules requiring sterically hindered thioether motifs. The stability imparted by the tert-butyl groups enhance

Used primarily as an intermediate in the synthesis of agrochemicals and pharmaceuticals, this compound serves as a building block for sulfur-containing organic molecules. Its chloro and tert-butylthio groups enable selective functionalization in cross-coupling reactions, making it valuable in the development of crop protection agents. It is also employed in research settings to design complex molecules requiring sterically hindered thioether motifs. The stability imparted by the tert-butyl groups enhances its utility in reaction pathways where decomposition is a concern.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...