(Phenylthio)acetyl chloride

95%

Reagent Code: #226708
fingerprint
CAS Number 7031-27-8

science Other reagents with same CAS 7031-27-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.66 g/mol
Formula C₆H₆SCH₂COCl
badge Registry Numbers
MDL Number MFCD00054471
thermostat Physical Properties
Boiling Point 115-116 °C at 3 Torr (lit.)
inventory_2 Storage & Handling
Density 1.258 g/mL at 25 °C (lit.)
Storage 2-8°C

description Product Description

Used primarily as a reagent in organic synthesis, particularly in the preparation of thioester derivatives. It serves as an acylating agent for introducing the (phenylthio)acetyl group into various nucleophilic compounds such as amines and alcohols. This functionality is valuable in the development of pharmaceutical intermediates, especially in the synthesis of sulfur-containing bioactive molecules. Its reactivity makes it useful in constructing complex molecular frameworks in medicinal chemistry and in the modification of peptides and heterocycles. Due to its sensitivity to moisture, it is typically handled under anhydrous conditions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿5,660.00
250mg
10-20 days ฿9,590.00
1g
10-20 days ฿25,850.00
(Phenylthio)acetyl chloride
No image available

Used primarily as a reagent in organic synthesis, particularly in the preparation of thioester derivatives. It serves as an acylating agent for introducing the (phenylthio)acetyl group into various nucleophilic compounds such as amines and alcohols. This functionality is valuable in the development of pharmaceutical intermediates, especially in the synthesis of sulfur-containing bioactive molecules. Its reactivity makes it useful in constructing complex molecular frameworks in medicinal chemistry and in

Used primarily as a reagent in organic synthesis, particularly in the preparation of thioester derivatives. It serves as an acylating agent for introducing the (phenylthio)acetyl group into various nucleophilic compounds such as amines and alcohols. This functionality is valuable in the development of pharmaceutical intermediates, especially in the synthesis of sulfur-containing bioactive molecules. Its reactivity makes it useful in constructing complex molecular frameworks in medicinal chemistry and in the modification of peptides and heterocycles. Due to its sensitivity to moisture, it is typically handled under anhydrous conditions.

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...