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About This Item
Linear Formula:
CH3(CH2)11P(C6H5)3Br
CAS Number:
Molecular Weight:
511.52
EC Number:
MDL number:
UNSPSC Code:
12352002
PubChem Substance ID:
Recommended Products
Assay
98%
reaction suitability
reaction type: C-C Bond Formation
mp
85-88 °C (lit.)
SMILES string
[Br-].CCCCCCCCCCCC[P+](c1ccccc1)(c2ccccc2)c3ccccc3
InChI
1S/C30H40P.BrH/c1-2-3-4-5-6-7-8-9-10-20-27-31(28-21-14-11-15-22-28,29-23-16-12-17-24-29)30-25-18-13-19-26-30;/h11-19,21-26H,2-10,20,27H2,1H3;1H/q+1;/p-1
InChI key
NSIFOGPAKNSGNW-UHFFFAOYSA-M
Application
Involved in comparative electrochemical studies of anticorrosion efficiency of nanocomposite coatings
Intercalating agent for modifying anticorrosion, gas barrier, mechanical and thermal properties of nanocomposite coatings
Mediator for reactions of nitrophenyl acetate
Studies of:
Intercalating agent for modifying anticorrosion, gas barrier, mechanical and thermal properties of nanocomposite coatings
Mediator for reactions of nitrophenyl acetate
Studies of:
- Nucleophilic substitution kinetics of sulfonate ester
- Intercalated polyester / silicate nanocomposites
- Thermal stability of quaternary phosphonium-modified montmorillonites in silicate layered polymer nanocomposites
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Meera Shanmuganathan et al.
Analytica chimica acta, 773, 24-36 (2013-04-09)
High quality assays are needed in drug discovery to reduce the high attrition rate of lead compounds during primary screening. Capillary electrophoresis (CE) represents a versatile micro-separation technique for resolution of enzyme-catalyzed reactions, including substrate(s), product(s), cofactor(s) and their stereoisomers
Ben C Chung et al.
Science (New York, N.Y.), 341(6149), 1012-1016 (2013-08-31)
MraY (phospho-MurNAc-pentapeptide translocase) is an integral membrane enzyme that catalyzes an essential step of bacterial cell wall biosynthesis: the transfer of the peptidoglycan precursor phospho-MurNAc-pentapeptide to the lipid carrier undecaprenyl phosphate. MraY has long been considered a promising target for
Yuzuru Itoh et al.
Science (New York, N.Y.), 340(6128), 75-78 (2013-04-06)
The 21st amino acid, selenocysteine (Sec), is synthesized on its cognate transfer RNA (tRNA(Sec)). In bacteria, SelA synthesizes Sec from Ser-tRNA(Sec), whereas in archaea and eukaryotes SepSecS forms Sec from phosphoserine (Sep) acylated to tRNA(Sec). We determined the crystal structures
Lisa M Willis et al.
Proceedings of the National Academy of Sciences of the United States of America, 110(51), 20753-20758 (2013-12-05)
Capsular polysaccharides (CPSs) are high-molecular-mass cell-surface polysaccharides, that act as important virulence factors for many pathogenic bacteria. Several clinically important Gram-negative pathogens share similar systems for CPS biosynthesis and export; examples include Escherichia coli, Campylobacter jejuni, Haemophilus influenzae, Neisseria meningitidis
Yuzuru Itoh et al.
Journal of molecular biology, 426(8), 1723-1735 (2014-01-25)
The 21st amino acid, selenocysteine (Sec), is incorporated translationally into proteins and is synthesized on its specific tRNA (tRNA(Sec)). In Bacteria, the selenocysteine synthase SelA converts Ser-tRNA(Sec), formed by seryl-tRNA synthetase, to Sec-tRNA(Sec). SelA, a member of the fold-type-I pyridoxal
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