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4-acetylphenyl 4-nitrobenzenesulfonate is a chemical compound with the molecular formula C14H11NO6S. It is an organic compound that features a 4-acetylphenyl group (a phenyl ring with an acetyl group attached to the 4-position) and a 4-nitrobenzenesulfonate group (a benzene ring with a nitro group and a sulfonate group attached to the 4-position). 4-acetylphenyl 4-nitrobenzenesulfonate is known for its potential applications in the synthesis of various pharmaceuticals and dyes, as well as its use as an intermediate in organic chemistry. Due to its complex structure, it is important to handle 4-acetylphenyl 4-nitrobenzenesulfonate with care, as it may have specific safety and disposal considerations.

55660-68-9

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55660-68-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55660-68-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,6,6 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 55660-68:
(7*5)+(6*5)+(5*6)+(4*6)+(3*0)+(2*6)+(1*8)=139
139 % 10 = 9
So 55660-68-9 is a valid CAS Registry Number.

55660-68-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-acetylphenyl 4-nitrobenzenesulfonate

1.2 Other means of identification

Product number -
Other names -

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

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

More Details:55660-68-9 SDS

55660-68-9Relevant academic research and scientific papers

Aryl and heteroaryl nosylates as stable and cheap partners for Suzuki-Miyaura cross-coupling reactions

Dikova, Anna,Cheval, Nicolas P.,Blanc, Aurélien,Weibel, Jean-Marc,Pale, Patrick

, p. 1960 - 1968 (2016/04/05)

Aryl and heteroaryl para-nitrophenylsulfonates (nosylates) have been successfully engaged for the first time in Suzuki-Miyaura cross-coupling reactions with various aryl or vinylboronic acids (48-98%, 12 examples). The best catalyst/ligand combination have been determined to be 2 mol % of palladium acetate (Pd(OAc)2) and 4 mol % of 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl (XPhos) using K3PO4 as base, in tetrahydrofuran at 80 °C. These new reaction conditions notably provide a direct and very efficient access to the natural alkaloid dubamine.

Kinetic study on alkaline hydrolysis of Y-substituted phenyl X-substituted benzenesulfonates: Effects of changing nucleophile from azide to hydroxide ion on reactivity and transition-state structure

Moon, Ji-Hyun,Kim, Min-Young,Han, So-Yeop,Um, Ik-Hwan

, p. 1563 - 1568 (2015/08/11)

Second-order rate constants (kOH-) for alkaline hydrolysis of 2,4-dinitrophenyl X-substituted benzenesulfonates (1a-1f) and Y-substituted phenyl 4-nitrobezenesulfonates (2a-2g) have been measured spectrophotometrically. Comparison of kOH/

Chemoselective regulation of TREK2 channel: Activation by sulfonate chalcones and inhibition by sulfonamide chalcones

Kim, Eun-Jin,Ryu, Hyung Won,Curtis-Long, Marcus J.,Han, Jaehee,Kim, Jun Young,Cho, Jung Keun,Kang, Dawon,Park, Ki Hun

supporting information; experimental part, p. 4237 - 4239 (2010/08/22)

Although it has not been extensively studied, a significant volume of literature suggests that TREK2 will probably turn out to be an important channel in charge of tuning neuronal transmitter and hormone levels. Thus, pharmacological tools which can manip

Sulfonate chalcone as new class voltage-dependent K+ channel blocker

Yarishkin, Oleg V.,Ryu, Hyung Won,Park, Jae-Yong,Yang, Min Suk,Hong, Seong-Geun,Park, Ki Hun

, p. 137 - 140 (2008/09/16)

Chalcone derivatives 1-17 were synthesized and their voltage-dependent K+ channel inhibitory activities were investigated. The effective K+ channel blockers were shown to be sulfonate chalcones 9-17, in which the sulfonyloxy group is

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