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Key Documents

564613

Sigma-Aldrich

5-Amino-2-nitrobenzoic acid

97%

Sinonimo/i:

2-Nitro-5-aminobenzoic acid, 3-Carboxy-4-nitroaniline, NSC 74455

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About This Item

Formula condensata:
H2NC6H3(NO2)CO2H
Numero CAS:
Peso molecolare:
182.13
Beilstein:
2107512
Numero CE:
Numero MDL:
Codice UNSPSC:
12352106
eCl@ss:
32160406
ID PubChem:
NACRES:
NA.22

Saggio

97%

Forma fisica

solid

Impiego in reazioni chimiche

reaction type: solution phase peptide synthesis

Punto di fusione

236-238 °C (lit.)

applicazioni

peptide synthesis

Stringa SMILE

Nc1ccc(c(c1)C(O)=O)[N+]([O-])=O

InChI

1S/C7H6N2O4/c8-4-1-2-6(9(12)13)5(3-4)7(10)11/h1-3H,8H2,(H,10,11)
KZZWQCKYLNIOBT-UHFFFAOYSA-N

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Applicazioni

Reactant for:
  • Two-component dendritic chain reactions
  • Enzymic activation of hydrophobic self-immolative dendrimers
  • Preparation of insulin receptor tyrosine kinase activator
  • Preparation of polymer-bound diazonium salts using Merrifield resin-bound piperazine

Pittogrammi

Flame over circle

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Ox. Sol. 2

Codice della classe di stoccaggio

5.1B - Oxidizing hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)


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Eran Sella et al.
Chemical communications (Cambridge, England), 46(35), 6575-6577 (2010-08-18)
A new dendritic chain reaction probe system was demonstrated to produce exponential signal amplification for the detection of sulfhydryl compounds.
L C Kirby et al.
Lipids, 30(9), 863-867 (1995-09-01)
Conjugated bile acid hydrolase (CBAH) refers to a class of enzymes which catalyze the cleavage of the amino acid moieties from conjugated bile acids. These enzymes are significant because of their role in providing substrates for further microbial metabolism in
Yu Jin Park et al.
Clinical biochemistry, 50(12), 719-725 (2017-03-05)
The use of iodinated contrast media has grown in popularity in the past two decades, but relatively little attention has been paid to the possible interferential effects of contrast media on laboratory test results. Herein, we investigate medical contrast media
Magdalena Wysocka et al.
Analytical biochemistry, 399(2), 196-201 (2010-01-16)
Previously selected by the combinatorial chemistry approach, potent fluorogenic substrate of proteinase 3 was used as the starting structure to design new substrates. The general formula of the synthesized peptides is as follows: ABZ-Tyr-Tyr-Abu-ANB-X-NH(2), where ANB (5-amino-2-nitrobenzoic acid) served as
F Schiele et al.
Clinical chemistry, 33(11), 1978-1982 (1987-11-01)
We describe the process of certification for a gamma-glutamyltransferase reference material (CRM no. 319). Fifteen laboratories participated to this interlaboratory evaluation. All steps of the measurements were controlled in an effort to locate potential sources of variations. In particular, the

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