3-Chloropropyl thiolacetate

technical grade, ≥90%

Reagent Code: #132500
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CAS Number 13012-54-9

science Other reagents with same CAS 13012-54-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 152.64 g/mol
Formula C₅H₉ClOS
badge Registry Numbers
MDL Number MFCD00001002
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of functionalized organosilanes for surface modification of materials like glass and polymers. It is also employed in the synthesis of specialty thiols through deprotection, where the thiolacetate group is hydrolyzed under mild conditions to release the free thiol. Its chloro and sulfur-containing functionality allows for sequential reactions, making it useful in the development of ligands, catalysts, and custom molecules in pharmaceutical and agrochemical research. Additionally, it finds use in polymer chemistry to introduce reactive side chains for crosslinking or further chemical modification.

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inventory 25g
10-20 days ฿11,200.00

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3-Chloropropyl thiolacetate
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Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of functionalized organosilanes for surface modification of materials like glass and polymers. It is also employed in the synthesis of specialty thiols through deprotection, where the thiolacetate group is hydrolyzed under mild conditions to release the free thiol. Its chloro and sulfur-containing functionality allows for sequential reactions, making it useful in the development of ligands, catalysts, and cust

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of functionalized organosilanes for surface modification of materials like glass and polymers. It is also employed in the synthesis of specialty thiols through deprotection, where the thiolacetate group is hydrolyzed under mild conditions to release the free thiol. Its chloro and sulfur-containing functionality allows for sequential reactions, making it useful in the development of ligands, catalysts, and custom molecules in pharmaceutical and agrochemical research. Additionally, it finds use in polymer chemistry to introduce reactive side chains for crosslinking or further chemical modification.

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