5-Bromnicotinsaeure

Bezeichnung:5-Bromnicotinsaeure

CAS-Nr20826-04-4

Englisch Name:5-Bromonicotinic acid

CBNumberCB3375701

SummenformelC6H4BrNO2

Molgewicht202.01

MOL-Datei20826-04-4.mol

Synonyma

5-Bromnicotinsaeure

5-Bromnicotinsaeure physikalisch-chemischer Eigenschaften

Schmelzpunkt	178-180 °C(lit.)
Siedepunkt	259.67°C (rough estimate)
Dichte	1.7477 (rough estimate)
Dampfdruck	0.01Pa at 25℃
Brechungsindex	1.6120 (estimate)
storage temp.	2-8°C
Löslichkeit	DMSO (Slightly), Methanol (Slightly)
pka	3.08±0.10(Predicted)
Aggregatzustand	Powder
Farbe	White to yellow-gray or light brown
BRN	115854
InChI	InChI=1S/C6H4BrNO2/c7-5-1-4(6(9)10)2-8-3-5/h1-3H,(H,9,10)
InChIKey	FQIUCPGDKPXSLL-UHFFFAOYSA-N
SMILES	C1=NC=C(Br)C=C1C(O)=O
LogP	1.17-1.29 at 23.5℃ and pH6.4
CAS Datenbank	20826-04-4(CAS DataBase Reference)

Sicherheit

Kennzeichnung gefährlicher	Xi
R-Sätze:	36/37/38
S-Sätze:	26-36-24/25
WGK Germany	3
RTECS-Nr.	QT0868000
HazardClass	IRRITANT
HS Code	29333999

Gefahreninformationscode (GHS)

5-Bromonicotinic acid Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:
R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.
S-Sätze Betriebsanweisung:
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.
S24/25:Berührung mit den Augen und der Haut vermeiden.
Chemische Eigenschaften
Light yellow Cryst
Verwenden
5-Bromopyridine-3-carboxylic acid (5-bromonicotinic acid) was used in the synthesis of 3-guanidinomethyl-5-iodopyridine.
Reaktionen
5-Bromonicotinic acid could used as starting material to synthesize 3-guanidinomethyl-5-iodopyridine. It is also used to prepare four novel multifunctional coordination compounds with different lanthanide(III) ions (Dy, Tb, Yb, and Nd). These materials possess different structures and dimensionalities and show interesting magnetic and luminescence properties, as well as a complete absence of cytotoxicity both in cancer and non-cancer Caco-2 cells[1-2].
Synthesis Reference(s)
Journal of the American Chemical Society, 70, p. 2381, 1948 DOI: 10.1021/ja01187a020
Synthese

29681-44-5

20826-04-4

General procedure for the synthesis of 5-bromonicotinic acid from methyl 5-bromonicotinate: to a solution of methyl 5-bromonicotinate (500 mg, 2.3 mmol) in tetrahydrofuran (THF, 5 mL) was added an aqueous 1 N sodium hydroxide solution (5 mL, 2.3 mmol). The reaction mixture was stirred at room temperature for 10 min. Subsequently, the reaction solution was acidified to pH 6 with acetic acid and then extracted three times with ethyl acetate. The organic phases were combined, dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give 5-bromonicotinic acid as a white solid (153 mg, 33% yield).
läuterung methode
The acid is recrystallised from H2O and then from EtOH using charcoal. The amide has m 219-219.5o (from aqueous EtOH), and the methyl ester, prepared by addition of ethereal diazomethane, can be purified by sublimation in a vacuum and has m 98-99o. The acid chloride also can be sublimed in vacuo and has m 74-75o and gives the methyl ester in MeOH. [Graf J Prakt Chem 138 244 1933, Bachman & Micucci J Am Chem Soc 70 2381 1948, Garcia et al. J Am Chem Soc 82 4430 1960, Misic-Vokovic et al. J Chem Soc 34 1978, Beilstein 22/2 V 181.]
Einzelnachweise
[1] Vaidyanathan G, et al. Iodopyridine-for-iodobenzene substitution for use with low molecular weight radiopharmaceuticals: application to m-iodobenzylguanidine. Bioconjugate Chemistry, 1998; 9: 758–764.
[2] Ruiz C, et al. Multifunctional coordination compounds based on lanthanide ions and 5-bromonicotinic acid: magnetic, luminescence and anti-cancer properties. CrystEngComm, 2019; 21: 3881-3890.

5-Bromonicotinic acid Upstream-Materialien And Downstream Produkte

5-Bromnicotinsaeure Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

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