What is the 4-NITRO-2-SULFOANILINE?

4-NITRO-2-SULFOANILINE is , while it's Molecular Formula is C6H6N2O5S. Used in Dye and Pigment Industry: 4-NITRO-2-SULFOANILINE is used as a chemical intermediate for the synthesis of dyes and pigments. Its ability to form colored compounds makes it a valuable component in the production of various dyes and pigments, which are widely used in coloring textiles, plastics, and other materials. Used in Pharmaceutical Industry: 4-NITRO-2-SULFOANILINE is used as a building block for the synthesis of pharmaceutical compounds. Its unique chemical structure allows it to be incorporated into various drug molecules, potentially leading to the development of new medications with improved therapeutic properties. Used in Analytical Chemistry: 4-NITRO-2-SULFOANILINE is used as a reagent in analytical chemistry for the detection and quantification of specific substances. Its chemical properties enable it to react with certain compounds, allowing for their identification and measurement in various samples. Used in Research and Development: 4-NITRO-2-SULFOANILINE is used as a research compound in the development of new chemical processes and materials. Its unique structure and properties make it an interesting subject for scientific investigation, potentially leading to new discoveries and innovations in various fields.

What is the CAS number for 4-NITRO-2-SULFOANILINE?

The CAS number of 4-NITRO-2-SULFOANILINE is 96-75-3.

What is 4-NITRO-2-SULFOANILINE (96-75-3) used for?

4-NITRO-2-SULFOANILINE, also known as 2-amino-4-nitrobenzenesulfonic acid, is an arenesulfonic acid derivative with a benzene ring structure. It is characterized by the presence of a sulfonic acid group, an amino group at the ortho position, and a nitro group at the para position. This unique chemical structure endows 4-NITRO-2-SULFOANILINE with various properties and potential applications in different industries.InChI:InChI=1/C6H6N2O5S/c7-5-2-1-4(8(9)10)3-6(5)14(11,12)13/h1-3H,7H2,(H,11,12,13)

What is the 4-NITRO-2-SULFOANILINE?

4-NITRO-2-SULFOANILINE is , while it's Molecular Formula is C6H6N2O5S. Used in Dye and Pigment Industry: 4-NITRO-2-SULFOANILINE is used as a chemical intermediate for the synthesis of dyes and pigments. Its ability to form colored compounds makes it a valuable component in the production of various dyes and pigments, which are widely used in coloring textiles, plastics, and other materials. Used in Pharmaceutical Industry: 4-NITRO-2-SULFOANILINE is used as a building block for the synthesis of pharmaceutical compounds. Its unique chemical structure allows it to be incorporated into various drug molecules, potentially leading to the development of new medications with improved therapeutic properties. Used in Analytical Chemistry: 4-NITRO-2-SULFOANILINE is used as a reagent in analytical chemistry for the detection and quantification of specific substances. Its chemical properties enable it to react with certain compounds, allowing for their identification and measurement in various samples. Used in Research and Development: 4-NITRO-2-SULFOANILINE is used as a research compound in the development of new chemical processes and materials. Its unique structure and properties make it an interesting subject for scientific investigation, potentially leading to new discoveries and innovations in various fields.

What is the CAS number for 4-NITRO-2-SULFOANILINE?

The CAS number of 4-NITRO-2-SULFOANILINE is 96-75-3.

What is 4-NITRO-2-SULFOANILINE (96-75-3) used for?

4-NITRO-2-SULFOANILINE, also known as 2-amino-4-nitrobenzenesulfonic acid, is an arenesulfonic acid derivative with a benzene ring structure. It is characterized by the presence of a sulfonic acid group, an amino group at the ortho position, and a nitro group at the para position. This unique chemical structure endows 4-NITRO-2-SULFOANILINE with various properties and potential applications in different industries.InChI:InChI=1/C6H6N2O5S/c7-5-2-1-4(8(9)10)3-6(5)14(11,12)13/h1-3H,7H2,(H,11,12,13)

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4-NITRO-2-SULFOANILINE

Name 4-NITRO-2-SULFOANILINE
CAS 96-75-3
Purity 99%

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Product Details

Top Quality 4-NITRO-2-SULFOANILINE 96-75-3 Hot Sell In Stock

Molecular Formula: C6H6N2O5S
Molecular Weight: 218.19
Melting Point: 196 °C(Solv: water (7732-18-5))
Refractive Index: 1.662
PKA: -1.01±0.36(Predicted)
PSA： 134.59000
Density: 1.727 g/cm³
LogP: 2.60890

4-NITRO-2-SULFOANILINE(Cas 96-75-3) Usage

Definition

ChEBI: The arenesulfonic acid that is benzenesulfonic acid substituted at the ortho position by an amino group and at the para posiion

InChI:InChI=1/C6H6N2O5S/c7-5-2-1-4(8(9)10)3-6(5)14(11,12)13/h1-3H,7H2,(H,11,12,13)

96-75-3 Relevant articles

Erratum: Integrated structure-based activity prediction model of benzothiadiazines on various genotypes of HCV NS5b polymerase (1a, 1b and 4) and its application in the discovery of new derivatives (Bioorganic and Medicinal Chemistry (2012) 20:7 (2455-2478))

Ismail, Mohamed A.H.,Abou El Ella, Dalal A.,Abouzid, Khaled A.M.,Mahmoud, Amr H.

supporting information, p. 5647 - 5647 (2013/09/02)

Development of an efficient ruthenium catalyzed synthetic process and mechanism for the facile conversion of benzothiazoles to orthanilic acids

Jagadeesh,Karthikeyan,Nithya,Sandhya, Y. Sree,Reddy, S. Sudhaker,Reddy, P. Pradeep Kumar,Kumar, M. Vinod,Charan, K.T. Prabhu,Narender,Bhagat

experimental part, p. 99 - 107 (2010/12/18)

Ruthenium-Schiff base complex catalyzed ...

Preparation, crystal structure and microwave studies on ring-substituted arylammonium hydrogen sulfate salts

Kapoor,Srivastava, Pratibha,Singh, Gurdip,Froehlich, Roland

, p. 1283 - 1288 (2008/09/18)

Three ring substituted arylammonium hydr...

Triazinyl reactive dyes containing additional fiber reactive groups bound through the sulfonylalkylaminoalkylamino bridge

-

, (2008/06/13)

The invention relates to novel useful re...

96-75-3 Process route

: 2942-06-5
6-nitrobenzo[d]thiazole

: 96-75-3
2-amino-5-nitro-benzenesulfonic acid

Conditions

Conditions	Yield
With [RuCl(P(C₆H₅)3)2(O(C₆H₄)NCH(C₄H₃N))]; bromamine B; sodium hydroxide; In water; acetonitrile; at 39.84 ℃; for 5.75h;	90%

active charcoal: active charcoal

: 2941-63-1
2-methyl-6-nitrobenzothiazole

: 96-75-3
2-amino-5-nitro-benzenesulfonic acid

Conditions

Conditions	Yield
With dihydrogen peroxide; In sodium hydroxide;

96-75-3 Upstream products

96-73-1
2-chloro-5-nitro-benzenesulfonic acid
100-01-6
4-nitro-aniline
7664-93-9
sulfuric acid
7553-56-2
iodine

96-75-3 Downstream products

51-28-5
2,4-Dinitrophenol
827-94-1
2,6-dibromo-4-nitroaniline
5398-27-6
2,6-diiodo-4-nitroaniline
861304-81-6
2-amino-3-iodo-5-nitro-benzenesulfonic acid

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