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113269-03-7

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  • N-[4-fluoro-2-[(4-methylphenyl)sulfonylamino]-5-nitrophenyl]-4-methylbenzenesulfonamide

    Cas No: 113269-03-7

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113269-03-7 Usage

General Description

1,2-DITOSYLAMINO-4-FLUORO-5-NITROBENZENE is a chemical compound that is commonly used in synthesis and organic chemistry. It is a derivative of nitrobenzene, with two tosylamino groups and one fluorine atom attached to the benzene ring. The compound has a molecular weight of 369.32 g/mol and a molecular formula of C14H12FNO4S2. It is often used as a reagent in the preparation of various organic compounds and can also be used in the production of pharmaceuticals and agrochemicals. 1,2-DITOSYLAMINO-4-FLUORO-5-NITROBENZENE is a versatile compound with a wide range of potential applications in the field of chemistry and chemical engineering.

Check Digit Verification of cas no

The CAS Registry Mumber 113269-03-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,2,6 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 113269-03:
(8*1)+(7*1)+(6*3)+(5*2)+(4*6)+(3*9)+(2*0)+(1*3)=97
97 % 10 = 7
So 113269-03-7 is a valid CAS Registry Number.
InChI:InChI=1/C20H18FN3O6S2/c1-13-3-7-15(8-4-13)31(27,28)22-18-11-17(21)20(24(25)26)12-19(18)23-32(29,30)16-9-5-14(2)6-10-16/h3-12,22-23H,1-2H3

113269-03-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[4-fluoro-2-[(4-methylphenyl)sulfonylamino]-5-nitrophenyl]-4-methylbenzenesulfonamide

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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More Details:113269-03-7 SDS

113269-03-7Relevant articles and documents

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THE FOUR 6-HALO-7-NITROQUINOXALINES

Nasielski-Hinkens, Raymonde,Leveque, Pierre,Castelet, Daniel,Nasielski, Jacques

, p. 2433 - 2442 (2007/10/02)

The study of relative nucleofugicities of nitro and halogen in quinoxalines required the synthesis of the four 6-halo-7-nitroquinoxalines 2a-d.The fluoro-, chloro- and bromo-derivatives were made from the commercially available or readily accessible 1,2-diamino-4-halobenzenes, using the nitration of the corresponding p-toluenesulfonamides.This scheme failed in the case of the iodo compound because of extensive nitro-deiodination.The synthesis of 6-iodo-7-nitroquinoxaline was finally achieved from m-fluoroiodobenzene by taking advantage of the high reactivity of fluorine, compared to iodine, in 2,4-dinitrohalobenzenes.

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