16192-07-7 Usage
Description
PROPARGYL P-TOLUENESULFONATE is an organic compound that features a propargyl group attached to a p-toluenesulfonate group. It is known for its potential genotoxic properties, which can impact both bacterial and mammalian cell systems.
Uses
Used in Chemical Synthesis:
PROPARGYL P-TOLUENESULFONATE is used as a protected propargyl compound for chemical synthesis, particularly in the creation of complex organic molecules. Its protective group allows for selective reactions and prevents unwanted side reactions during the synthesis process.
Used in Pharmaceutical Research:
In the pharmaceutical industry, PROPARGYL P-TOLUENESULFONATE is used as a research compound for studying its genotoxic effects on bacterial and mammalian cell systems. This helps in understanding its potential applications and limitations in drug development and designing safer and more effective medications.
Used in Material Science:
PROPARGYL P-TOLUENESULFONATE may also find applications in material science, where its unique chemical properties can be utilized to develop new materials with specific characteristics, such as improved stability or reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 16192-07-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,1,9 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 16192-07:
(7*1)+(6*6)+(5*1)+(4*9)+(3*2)+(2*0)+(1*7)=97
97 % 10 = 7
So 16192-07-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H10O2S/c1-3-8-13(11,12)10-6-4-9(2)5-7-10/h1,4-7H,8H2,2H3
16192-07-7Relevant articles and documents
Creating Dynamic Nanospaces in Solution by Cationic Cages as Multirole Catalytic Platform for Unconventional C(sp)?H Activation Beyond Enzyme Mimics
Li, Kang,Wu, Kai,Lu, Yu-Lin,Guo, Jing,Hu, Peng,Su, Cheng-Yong
supporting information, (2021/12/14)
Herein we demonstrate that, based on the creation of dynamic nanospaces in solution by highly charged positive coordination cage of [Pd6(RuL3)8]28+, multirole and multi-way cage-confined catalysis is accomplisha
INHIBITORS OF HEPATITIS C VIRUS
-
Page/Page column 181, (2012/05/19)
A class of compounds that inhibit Hepatitis C Virus (HCV) is disclosed, along with compositions containing the compound, and methods of using the composition for treating individuals infected with HCV.
Synthesis of thiophenes from allenyl sulfones involving α,β-unsaturated sulfines as intermediates
Linden, Johannes B. van der,Asten, Peter F. T. M. van,Braverman, Samuel,Zwanenburg, Binne
, p. 51 - 60 (2007/10/02)
The synthesis of thiophenes starting from allenyl sulfones, via intermediate formation of α,β-unsaturated sulfines, is described.The allenyl sulfones were synthesized by a -sigmatropic rearrangement of appropriately substituted prop-2-ynyl sulfinates