702-13-6 Usage
Description
1-fluoro-4-(propan-2-ylsulfanyl)benzene is a chemical compound with the molecular formula C9H11FS. It is a colorless liquid with a distinct aromatic odor and is commonly used as an intermediate in organic synthesis. As a fluorobenzene derivative with a thiol group attached to the second carbon of the benzene ring, it is classified as a thioether.
Uses
Used in Pharmaceutical Industry:
1-fluoro-4-(propan-2-ylsulfanyl)benzene is used as an intermediate in the synthesis of various pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
1-fluoro-4-(propan-2-ylsulfanyl)benzene is also utilized in the production of agrochemicals, where it serves as an intermediate for the synthesis of various agricultural chemicals. Its role in this industry is crucial for the development of effective and environmentally friendly products.
Used in Fine Chemicals Production:
1-fluoro-4-(propan-2-ylsulfanyl)benzene is employed in the synthesis of other fine chemicals, which are high-purity, high-value chemicals used in various industries, including cosmetics, fragrances, and specialty chemicals.
Used as a Reagent in Organic Reactions:
In the field of organic chemistry, 1-fluoro-4-(propan-2-ylsulfanyl)benzene is used as a reagent in various organic reactions. Its unique properties make it a valuable tool for chemists in conducting research and developing new chemical processes.
Used in Chemical Industry for Product Manufacturing:
1-fluoro-4-(propan-2-ylsulfanyl)benzene is also used in the manufacture of various products within the chemical industry. Its versatility and reactivity contribute to the production of a wide range of chemical products.
Safety Note:
It is important to handle 1-fluoro-4-(propan-2-ylsulfanyl)benzene with caution as it can be hazardous if not used properly. Proper safety measures and handling procedures should be followed to ensure the safety of individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 702-13-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,0 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 702-13:
(5*7)+(4*0)+(3*2)+(2*1)+(1*3)=46
46 % 10 = 6
So 702-13-6 is a valid CAS Registry Number.
702-13-6Relevant articles and documents
Sulfonium ylide formation and subsequent C[sbnd]S bond cleavage of aromatic isopropyl sulfide catalyzed by hemin in aqueous solvent
Yan, Xiaojing,Li, Chang,Xu, Xiaofei,He, Quan,Zhao, Xiaoyong,Pan, Yuanjiang
supporting information, p. 3081 - 3087 (2019/05/08)
Heme is an abundant and widely existed cofactor for a variety of metalloenzymes, whose broader use is generally impeded by its high instability and poor solubility. Here we report an environment-benign and efficient strategy for the sulfonium ylide formation and subsequent C[sbnd]S bond cleavage of aromatic isopropyl sulfides, which was catalyzed by hemin in assistance of Triton X-100. This aqueous catalytic system exhibited good functional group tolerance to a variety of sulfides and diazo esters. And the reaction mechanism was preliminarily proposed on the basis of designed reactions. Furthermore, the cleavage of C[sbnd]S bond followed by introducing a functional ester group to aromatic sulfides, may potentially be employed for the late stage functionalization (LSF) of organosulfur drug in the future.
