thionitrobenzoic acid

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Factory Export Top Purity thionitrobenzoic acid 15139-21-6 In Stock

  • Molecular Formula:C7H5NO4S
  • Molecular Weight:199.187
  • Vapor Pressure:8.87E-08mmHg at 25°C 
  • Refractive Index:1.682 
  • Boiling Point:419.2 °C at 760 mmHg 
  • Flash Point:207.4 °C 
  • PSA:121.92000 
  • Density:1.575 g/cm3 
  • LogP:2.10490 

thionitrobenzoic acid(Cas 15139-21-6) Usage

General Description

Thionitrobenzoic acid, also known as 2-Nitrobenzenethiol, is a compound with the chemical formula C7H5NO3S. It is a yellow crystalline solid that is commonly used in organic synthesis and as a reagent in chemical reactions. Thionitrobenzoic acid is known for its use as a colorimetric reagent for the detection of various metal ions, such as copper, mercury, and zinc. It is also used in the determination of the concentration of proteins in biological samples. Thionitrobenzoic acid has a strong odor and is toxic if ingested or inhaled, and can cause irritation to the skin and eyes. Due to its potential hazards, it should be handled and stored with caution.

InChI:InChI=1/C7H5NO4S/c9-7(10)5-3-4(13)1-2-6(5)8(11)12/h1-3,13H,(H,9,10)

15139-21-6 Relevant articles

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Allium plants including garlic (Allium s...

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Entamoeba histolytica thioredoxin reductase: Molecular and functional characterization of its atypical properties

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Background: Entamoeba histolytica, an in...

Effect of N-B transition on the microenvironment surrounding 34Cys in human serum albumin

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The effect of pH on the microenvironment...

Protein Reduction and Dialysis-Free Work-Up through Phosphines Immobilized on a Magnetic Support: TCEP-Functionalized Carbon-Coated Cobalt Nanoparticles

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Characterization and in vitro functional analysis of thioredoxin glutathione reductase from the liver fluke Opisthorchis viverrini

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, p. 10148 - 10154 (2013)

We report the synthesis of atomically mo...

CENTA as a chromogenic substrate for studying β-lactamases

Bebrone, Carine,Moali, Catherine,Mahy, Florence,Rival, Sandrine,Docquier, Jean Denis,Rossolini, Gian Maria,Fastrez, Jacques,Pratt, Rex F.,Frere, Jean-Marie,Galleni, Moreno

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The plausible nitric oxide (NO)-sensing ...

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Atomically precise thiolate-protected no...

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Dynamics of the Cleavage of Ellman's Reagent in Surfactant Vesicles

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The cleavage of Ellman's reagent to 2-n...

Enzymatic spectrophotometric method for aflatoxin B detection based on acetylcholinesterase inhibition

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Molecular tubes with hydrogen bonding do...

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Study of the thiol/disulfide redox systems of the anaerobe Desulfovibrio vulgaris points out pyruvate:ferredoxin oxidoreductase as a new target for thioredoxin

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, p. 7812 - 7821 (2011)

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Highly sensitive DNA methylation analysis at CpG resolution by surface-enhanced Raman scattering via ligase chain reaction

Wang, Yuling,Wee, Eugene J. H.,Trau, Matt

, p. 10953 - 10956 (2015)

Sensitive and accurate DNA methylation a...

One-step electrochemically deposited gold nanoparticles interface grafted with avidin for acetylcholinesterase biosensor design

Zhang, Weiying,Ding, Jiawang,Qin, Yuehua,Liu, Deli,Du, Dan

, p. 5685 - 5691 (2010)

In this study, an interface embedded in ...

Novel solid-phase reagents for facile formation of intramolecular disulfide bridges in peptides under mild conditions

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, p. 7226 - 7238 (1998)

The controlled formation of intramolecul...

Characterization of an NADH-dependent persulfide reductase from shewanella loihica PV-4: Implications for the mechanism of sulfur respiration via FAD-dependent enzymes

Warner, Megan D.,Lukose, Vinita,Lee, Kyu Hyun,Lopez, Karlo,H. Sazinsky, Matthew,Crane, Edward J.

, p. 194 - 206 (2011)

The NADH-dependent persulfide reductase ...

Synthesis, characterization and biological activity of bis[3-ethyl-4-aryl-5-(2-methoxypyridin-5-yl)-1-propyl-1,3-dihydro-2H-imidazol-2-ylidene]gold(i) complexes

Gallati, Caroline Marie,Goetzfried, Sina Katharina,Ortmeier, Anna,Sagasser, Jessica,Wurst, Klaus,Hermann, Martin,Baecker, Daniel,Kircher, Brigitte,Gust, Ronald

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, (2021/12/22)

Nanozyme-based chemodynamic therapy (CDT...

15139-21-6 Process route

2-mercaptoethylamine hydrochloride
156-57-0

2-mercaptoethylamine hydrochloride

S-<(3-carboxy-4-nitrophenyl)thio>-2-aminoethanethiol
71899-86-0

S-<(3-carboxy-4-nitrophenyl)thio>-2-aminoethanethiol

2,2'-dithio-bis[ethylamine]
51-85-4

2,2'-dithio-bis[ethylamine]

5-thio-2-nitrobenzoic acid
15139-21-6

5-thio-2-nitrobenzoic acid

Conditions
Conditions Yield
With ethylenediaminetetraacetic acid; MES buffer; Rate constant; ionic strength dependency;
5-(1,2-Dicyano-ethylsulfanyl)-2-nitro-benzoic acid

5-(1,2-Dicyano-ethylsulfanyl)-2-nitro-benzoic acid

5-thio-2-nitrobenzoic acid
15139-21-6

5-thio-2-nitrobenzoic acid

1,2-Dicyanoethylene
764-42-1

1,2-Dicyanoethylene

Conditions
Conditions Yield
piperidine; In water; dimethyl sulfoxide; at 25 ℃; Rate constant; elimination, other bases;

15139-21-6 Upstream products

  • 921-01-7
    921-01-7

    rac-cysteine

  • 69-78-3
    69-78-3

    5,5'-dithiobis-(2-nitrobenzoic acid)

  • 52-90-4
    52-90-4

    L-Cysteine

  • 149997-68-2
    149997-68-2

    5-(2-cyanoethyldithio)-2-nitrobenzoic acid

15139-21-6 Downstream products

  • 69-78-3
    69-78-3

    5,5'-dithiobis-(2-nitrobenzoic acid)

  • 75-65-0
    75-65-0

    tert-butyl alcohol

  • 80072-86-2
    80072-86-2

    (6R,7R)-3-(((3-carboxy-4-nitrophenyl)thio)methyl)-8-oxo-7-(2-(thiophen-2-yl)acetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

  • 157930-09-1
    157930-09-1

    6-Mercaptopurine

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