4911-65-3 Usage
Description
3-Chloropropyl phenyl sulfide, with the molecular formula C9H11ClS, is a chemical compound that exists as a clear, colorless liquid with a pungent odor. It serves as an intermediate in the synthesis of various organic compounds and is utilized in the production of pharmaceuticals, pesticides, and specialty chemicals. Due to its potential to cause skin and eye irritation as well as respiratory issues, it is crucial to exercise proper safety measures when handling this chemical.
Uses
Used in Pharmaceutical Industry:
3-Chloropropyl phenyl sulfide is used as a key intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs and improving the efficacy of existing medications.
Used in Pesticide Industry:
In the pesticide sector, 3-chloropropyl phenyl sulfide is employed as an intermediate for the production of various pesticides, enhancing their effectiveness in controlling pests and protecting crops.
Used in Specialty Chemicals:
3-Chloropropyl phenyl sulfide is utilized in the manufacturing of specialty chemicals, where it plays a crucial role in the development of unique chemical products with specific applications.
Used as a Reagent in Organic Synthesis:
This chemical compound also serves as a reagent in organic synthesis reactions, facilitating the creation of new compounds and contributing to advancements in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 4911-65-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,1 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4911-65:
(6*4)+(5*9)+(4*1)+(3*1)+(2*6)+(1*5)=93
93 % 10 = 3
So 4911-65-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H11ClS/c10-7-4-8-11-9-5-2-1-3-6-9/h1-3,5-6H,4,7-8H2
4911-65-3Relevant articles and documents
Increasing Complexity: A Practical Synthetic Approach to Three-Dimensional, Cyclic Sulfoximines and First Insights into Their in Vitro Properties
Boulard, Emilie,Ganzer, Ursula,Lücking, Ulrich,Lienau, Philip,Oertel, Luisa,Sch?fer, Martina,Zibulski, Vivien
, (2020/03/23)
A short synthetic approach with broad scope to access five- to seven-membered cyclic sulfoximines in only two to three steps from readily available thiophenols is reported. Thus, simple building blocks were converted to complex molecular structures by a s
Pummerer Synthesis of Chromanes Reveals a Competition between Cyclization and Reductive Chlorination
Acosta-Guzmán, Paola,Rodríguez-López, Alvaro,Gamba-Sánchez, Diego
supporting information, p. 6903 - 6908 (2019/09/30)
The competition between an unprecedented reductive chlorination and the Pummerer reaction was studied and applied to the synthesis of benzofused oxygen heterocycles including 3-aminochromanes and in the intramolecular chlorination of activated aromatic ri
Scandium(III) Triflate-Catalyzed anti-Markovnikov Hydrothiolation of Functionalized Olefins
Kuciski, Krzysztof,Pawluc, Piotr,Hreczycho, Grzegorz
, p. 3936 - 3942 (2016/01/25)
Scandium(III) triflate promoted highly selective addition of thiols to functionalized olefins under mild conditions. The addition follows anti-Markovnikov regioselectivities, which are unusual for Lewis acids-catalyzed hydrothiolation. This reaction marks broad functional groups tolerance, which opens a beneficial synthetic route to functionalized and biologically active thio-compounds. This method is broadly applicable and offers a simple work-up in the green manner.
