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Sku CI26924_250_G
Chem Impex
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Product Information

Product Name
o-Phenyl chlorothiocarbonate
Brand Name
Chem Impex
Product Number
26924
CAS
1005-56-7
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
70498
IUPAC Name
O-phenyl chloromethanethioate
InChI Key
KOSYAAIZOGNATQ-UHFFFAOYSA-N
SMILES
C1=CC=C(C=C1)OC(=S)Cl

Description

o-Phenyl chlorothiocarbonate is widely utilized in research focused on:

Organic Synthesis: This compound serves as an effective reagent for the synthesis of various organic compounds, particularly in the formation of thiocarbonates, which are valuable intermediates in chemical manufacturing.

Pesticide Development: It plays a role in the formulation of certain pesticides, offering enhanced efficacy against pests while being less harmful to beneficial insects compared to traditional compounds.

Pharmaceutical Applications: Researchers use it in drug development processes to create thiol-containing pharmaceuticals, which can improve drug solubility and bioavailability.

Polymer Chemistry: This chemical is utilized in the production of specialty polymers, particularly those that require specific functional groups for enhanced performance in applications like coatings and adhesives.

Analytical Chemistry: It is employed as a derivatizing agent in analytical techniques, aiding in the detection and quantification of various analytes in complex mixtures, thus improving the accuracy of analytical results.

References Data Source From Pubchem

Chemical Synthesis of Homogeneous Glycoproteins for the Elucidation of Glycan Functions

Publication Name: The Molecular Immunology of Complex Carbohydrates - 4
Publication Date: 2026
DOI: 10.1007/978-3-032-04153-1_33

Biosynthesis of ergothioneine: current state, achievements, and perspectives

Publication Name: Applied Microbiology and Biotechnology
Publication Date: 2025-04-12
DOI: 10.1007/s00253-025-13476-4

Clean and Green Synthesis of Organic Isothiocyanates Using Zinc Peroxide as Desulfurizing Agent and Their Antimicrobial Activity

Publication Name: Russian Journal of Organic Chemistry
Publication Date: 2023-12
DOI: 10.1134/s1070428023120199

Sigmatropic rearrangements of B(MIDA)-propargylic alcohols towards the diverse synthesis of α-functionalized organoborons

Publication Name: Science China Chemistry
Publication Date: 2023-10-30
DOI: 10.1007/s11426-023-1722-8

Total Synthesis of Indolizidine Alkaloid (±)-Bipolamine I

Publication Name: Synfacts
Publication Date: 2022-09-20
DOI: 10.1055/s-0042-1752951