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75618-25-6

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75618-25-6 Usage

General Description

Butyl triflate, also known as trifluoromethanesulfonate, is a chemical compound with the formula C4H9CF3O3S. It is a colorless liquid that is commonly used as a reagent in organic synthesis. Butyl triflate is a powerful electrophile due to the presence of the triflate group, making it useful for a variety of reactions including alkylations, eliminations, and rearrangements. It is also used as a catalyst and as a versatile building block in the production of pharmaceuticals and agrochemicals. However, butyl triflate is highly reactive and should be handled with caution due to its potential to cause severe skin and eye irritation, as well as adverse effects on the respiratory system if inhaled.

Check Digit Verification of cas no

The CAS Registry Mumber 75618-25-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,6,1 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 75618-25:
(7*7)+(6*5)+(5*6)+(4*1)+(3*8)+(2*2)+(1*5)=146
146 % 10 = 6
So 75618-25-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H9F3O3S/c1-2-3-4-11-12(9,10)5(6,7)8/h2-4H2,1H3

75618-25-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Butyl Trifluoromethanesulfonate

1.2 Other means of identification

Product number -
Other names n-C4H9OSO2CF3

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:75618-25-6 SDS

75618-25-6Relevant articles and documents

A SIMPLE SYNTHESIS OF ALLYLSILANES VIA TRISBORANE

Wang, Kung K.,Dhumrongvaraporn, Sujitra

, p. 1007 - 1010 (1987)

Allylsilanes were prepared by protonation or alkylation of lithium 1-alkynyltrisborates followed by protonolysis or treatment with aqueous sodium hydroxide and iodine.

Tuning the biological activity of cationic anthraquinone analogues specifically toward Staphylococcus aureus

Subedi, Yagya Prasad,Alfindee, Madher N.,Shrestha, Jaya P.,Chang, Cheng-Wei Tom

, p. 683 - 690 (2018/08/23)

Development of new antibacterial agents against drug resistant bacteria is an imminent task, especially against methicillin-resistant Staphylococcus aureus (MRSA). While MRSA can still be treated with broad spectrum antibiotics, the use of which often leads to the disruption of normal microbial flora leading to Clostridium difficile infection (CDI). Herein, a new class of antibacterial agent, cationic anthraquinone analogues specifically against MRSA, has been developed. Through the variation and optimization of substituents, these agents are selective toward MRSA, and not Gram negative bacteria which may avoid the problem of CDI. In addition, newly discovered lead compounds also show significantly reduced cytotoxicity against normal mammalian cells than cancerous cells. This interesting finding can alleviate the toxicity and side effect problems often associate with the use of antibiotics.

DERIVATIVES OF ELASTIN-LIKE POLYPEPTIDES AND USES THEREOF

-

Page/Page column 18, (2017/02/28)

The present invention concerns the use of a thioether alkylation process for modulating the lower critical solution temperature of an elastin-like polypeptide comprising at least one methionine residue. It also concerns derivatives of elastin-like polypeptides and their preparation process.

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