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16192-07-7

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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

16192-07-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name PROPARGYL P-TOLUENESULFONATE

1.2 Other means of identification

Product number -
Other names m-Toluenesulfonicacidpropargylester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:16192-07-7 SDS

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

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