702-13-6 Usage
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 academic research and scientific papers
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.
2-(3,5-DISUBSTITUTEDPHENYL)PYRIMIDIN-4(3H)-ONE DERIVATIVES
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Page/Page column 40, (2012/01/06)
O N NH R3 R2 O R1 168 ABSTRACT The present invention provides a 2-(3,5-disubstitutedphenyl)pyrimidin- 4(3H)-one compound of Formula (I) 5 (I) or a pharmaceutically acceptable salt thereof wherein R 1, R2 and R3 are as defined herein. The compounds of Formula (I) have been found to act as glucokinase activators. Consequently, the compounds of Formula (I) and 10 the pharmaceutical compositions thereof are useful for the treatment of diseases, disorders, or conditions mediated by glucokinase.
