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2-methylphenyl 3-nitrobenzenesulfonate is an organic compound with the chemical formula C13H11NO5S. It is a derivative of benzene, featuring a methyl group (-CH3) attached to the 2nd carbon atom and a nitro group (-NO2) at the 3rd position of the benzene ring. The molecule also contains a sulfonate group (-SO3H) attached to the 3-nitrobenzene moiety, which imparts acidic properties to the compound. This chemical is primarily used as an intermediate in the synthesis of various pharmaceuticals, dyes, and other organic compounds. Due to its reactivity and potential applications, it is essential to handle 2-methylphenyl 3-nitrobenzenesulfonate with care, as it may pose health and environmental risks.

5279-08-3

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5279-08-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5279-08-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,7 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5279-08:
(6*5)+(5*2)+(4*7)+(3*9)+(2*0)+(1*8)=103
103 % 10 = 3
So 5279-08-3 is a valid CAS Registry Number.

5279-08-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-methylphenyl) 3-nitrobenzenesulfonate

1.2 Other means of identification

Product number -
Other names 2-methylphenyl 3-nitrobenzenesulfonate

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:5279-08-3 SDS

5279-08-3Relevant academic research and scientific papers

ALKYLUREA DERIVATIVES ACTIVE AGAINST CANCER CELLS

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Page/Page column 24; 44, (2012/11/07)

Compounds of formula (I) : wherein A, m, n, R1, X, Y, R2, R3, R4, R5 and R6, as defined herein are provided as useful for the treatment of cancer or for the manufacture of anti-cancer agents.

Synthesis, biological evaluation, and structure-activity relationships of novel substituted N-phenyl ureidobenzenesulfonate derivatives blocking cell cycle progression in s-phase and inducing DNA double-strand breaks

Turcotte, Vanessa,Fortin, Sébastien,Vevey, Florence,Coulombe, Yan,Lacroix, Jacques,C?té, Marie-France,Masson, Jean-Yves,C.-Gaudreault, René

experimental part, p. 6194 - 6208 (2012/08/27)

Twenty-eight new substituted N-phenyl ureidobenzenesulfonate (PUB-SO) and 18 N-phenylureidobenzenesulfonamide (PUB-SA) derivatives were prepared. Several PUB-SOs exhibited antiproliferative activity at the micromolar level against the HT-29, M21, and MCF-

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