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A propos de cet article
Formule empirique (notation de Hill) :
C12H24BrN3P · F6P
Numéro CAS:
Poids moléculaire :
466.18
UNSPSC Code:
12352107
NACRES:
NA.22
MDL number:
Assay:
≥98.0% (HPLC)
Form:
powder
Service technique
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product line
Novabiochem®
assay
≥98.0% (HPLC)
form
powder
reaction suitability
reaction type: Coupling Reactions
manufacturer/tradename
Novabiochem®
mp
>100 °C
application(s)
peptide synthesis
storage temp.
2-8°C
SMILES string
F[P-](F)(F)(F)(F)F.[P+](Br)(N3CCCC3)(N2CCCC2)N1CCCC1
InChI
1S/C12H24BrN3P.F6P/c13-17(14-7-1-2-8-14,15-9-3-4-10-15)16-11-5-6-12-16;1-7(2,3,4,5)6/h1-12H2;/q+1;-1
InChI key
CYKRMWNZYOIJCH-UHFFFAOYSA-N
General description
A superior reagent for rapid and effective coupling of N-methyl amino acids with low enantiomerization and for other critical applications [1,2,3,4,5,6,7,8]. The coupling of N-methyl amino acids is difficult, and usually only gives low to moderate yields of products which are often contaminated with unwanted diastereomers. Many coupling reagents are ineffective or not practical to use: BOP and HOBt are often useless; BOP-Cl, pivaloyl chloride and Dpp-Cl require long reaction times and preactivation at 0°C.For coupling γ-aminoisobutyric acid (Aib), PyBrOP® is most effective when used with dimethylaminopyridine (DMAP) [3].
Associated Protocols and Technical Articles
Guide to Selection of Coupling Reagents
Literature references
[1] J. Coste, et al. in ′Peptides, Chemistry, Structure & Biology, Proc. 11th American Peptide Symposium′, J. E. Rivier & G. R. Marshall (Eds), ESCOM, Leiden, 1990, pp. 900.
[2] J. Coste, et al. (1990) Tetrahedron Lett., 31, 669.
[3] J. Coste, et al. in ′Peptides 1990, Proc. 21st European Peptide Symposium′, E. Giralt & D. Andreu (Eds), ESCOM, Leiden, 1990, pp. 76.
[4] J. Coste, et al. (1991) Tetrahedron Lett., 32, 1967.
[5] P. W. Baures, et al. (1997) J. Peptide Res., 50, 1.
[6] T. Doi, et al. (1999) Synlett, 11, 1751.
[7] A. M. Boldi, et al. (2001) J. Comb. Chem., 3, 367.
[8] S. Gazal, et al. (2001) J. Peptide Res., 58, 527.
Associated Protocols and Technical Articles
Guide to Selection of Coupling Reagents
Literature references
[1] J. Coste, et al. in ′Peptides, Chemistry, Structure & Biology, Proc. 11th American Peptide Symposium′, J. E. Rivier & G. R. Marshall (Eds), ESCOM, Leiden, 1990, pp. 900.
[2] J. Coste, et al. (1990) Tetrahedron Lett., 31, 669.
[3] J. Coste, et al. in ′Peptides 1990, Proc. 21st European Peptide Symposium′, E. Giralt & D. Andreu (Eds), ESCOM, Leiden, 1990, pp. 76.
[4] J. Coste, et al. (1991) Tetrahedron Lett., 32, 1967.
[5] P. W. Baures, et al. (1997) J. Peptide Res., 50, 1.
[6] T. Doi, et al. (1999) Synlett, 11, 1751.
[7] A. M. Boldi, et al. (2001) J. Comb. Chem., 3, 367.
[8] S. Gazal, et al. (2001) J. Peptide Res., 58, 527.
Analysis Note
Color (visual): white to slight yellow to beige
Appearance of substance (visual): powder
Identity (IR): passes test
Assay (HPLC, area%): ≥ 98.0 % (a/a)
Appearance of substance (visual): powder
Identity (IR): passes test
Assay (HPLC, area%): ≥ 98.0 % (a/a)
Other Notes
Replaces: 01-62-0017
Legal Information
Novabiochem is a registered trademark of Merck KGaA, Darmstadt, Germany
PyBroP is a registered trademark of Merck KGaA, Darmstadt, Germany
Mot-clé
Danger
Codes de danger
Que se passe-t-il ?
WGK 3
Point d'éclair (°F)
No data available
Mentions de précaution
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B
Classe de stockage
8A - Combustible corrosive hazardous materials
Point d'éclair (°C)
No data available
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