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Benzenemethanesulfonic acid, 4-nitro-, phenyl ester, also known as 4-nitrobenzenemethanesulfonic acid phenyl ester, is an organic compound with the chemical formula C13H11NO5S. It is a derivative of benzenemethanesulfonic acid, featuring a nitro group at the 4-position and a phenyl ester group attached to the sulfonic acid. Benzenemethanesulfonic acid, 4-nitro-, phenyl ester is characterized by its yellow crystalline appearance and is soluble in organic solvents. It is primarily used in the synthesis of various pharmaceuticals and chemical intermediates, particularly in the production of certain dyes and agrochemicals. Due to its reactivity and potential applications, it is an important compound in the field of organic chemistry.

53992-04-4

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53992-04-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53992-04-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,9,9 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 53992-04:
(7*5)+(6*3)+(5*9)+(4*9)+(3*2)+(2*0)+(1*4)=144
144 % 10 = 4
So 53992-04-4 is a valid CAS Registry Number.

53992-04-4SDS

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 phenyl (4-nitrophenyl)methanesulfonate

1.2 Other means of identification

Product number -
Other names Benzenemethanesulfonic acid,4-nitro-,phenyl ester

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:53992-04-4 SDS

53992-04-4Downstream Products

53992-04-4Relevant academic research and scientific papers

ALKANESULFONYLATION.XX. CATALYSIS OF THE PHENOLYSIS OF ALKANESULFONYL CHLORIDES IN PROTON-INERT MEDIA CATALYZED BY PYRIDINE BASES. THE EFFECT OF THE SUBSTRATE STRUCTURE

Skrypnik, Yu. G.,Lyashchuk, S. N.

, p. 695 - 700 (2007/10/02)

The kinetics of the reaction of methane-, ethane-, propane-, 1-methylmethane-, and cyclohexanesulfonyl chlorides and also of substituted phenylmethanesulfonyl chlorides with phenol in the presence of pyridine in chlorobenzene at 303 K were studied by GLC

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