165816
11-Bromoundecanoic acid
technical grade, 95%
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About This Item
Formula condensata:
Br(CH2)10COOH
Numero CAS:
Peso molecolare:
265.19
Beilstein:
1767205
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Grado
technical grade
Saggio
95%
P. ebollizione
173-174 °C/2 mmHg (lit.)
Punto di fusione
45-48 °C (lit.)
Gruppo funzionale
bromo
carboxylic acid
Stringa SMILE
OC(=O)CCCCCCCCCCBr
InChI
1S/C11H21BrO2/c12-10-8-6-4-2-1-3-5-7-9-11(13)14/h1-10H2,(H,13,14)
IUDGNRWYNOEIKF-UHFFFAOYSA-N
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Descrizione generale
11-Bromoundecanoic acid reacts with potassium salt of dimethyl hydantoin to yield 4,4-dimethyl hydantoin-undecanoic acid.
Applicazioni
11-Bromoundecanoic acid was used in the synthesis of 11-phenoxyundecyl phosphate and 11-hydroxytetradecanoic acid.
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 1
Punto d’infiammabilità (°F)
235.4 °F - closed cup
Punto d’infiammabilità (°C)
113 °C - closed cup
Dispositivi di protezione individuale
Eyeshields, Gloves, type N95 (US)
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I clienti hanno visto anche
Revathi V Padmanabhuni et al.
Industrial & engineering chemistry research, 51(14), 5148-5156 (2012-09-04)
The purpose of this study was to demonstrate that the surface of CaCO(3) fillers could be coated with an N-halamine based fatty acid to make the filler surface organophilic and accomplish antibacterial activity simultaneously, rendering the resulting polymer-filler composites antimicrobial.
I Navarro et al.
Bioorganic & medicinal chemistry, 4(3), 439-443 (1996-03-01)
The synthesis of deuterium labeled 11- and 12-hydroxytetradecanoic acids to study a (11E) desaturase in the moth Spodoptera littoralis is reported. [14,14,14-2H3] 12-hydroxytetradecanoic acid was synthesized in four steps from 11-iodo-1-undecene in 49% overall yield. Deuterium was introduced by reaction
L L Danilov et al.
Bioorganicheskaia khimiia, 35(3), 431-432 (2009-07-22)
A new scheme of synthesis of 11-phenoxyundecyl phosphate from 11-bromoundecanoic acid was suggested for its ability to react as an acceptor of 2-acetamido-2-deoxy-alpha-D-glucopyranosyl phosphate in a reaction catalyzed by UDP-N-acetylglucosamine : polyprenyl phosphate N-acetylglucosamine phosphotransferase from Salmonella arizona O:59.
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