52427
Butyl 4-nitrophenyl hexylphosphonate
≥95.0% (HPLC)
Synonym(s):
Hexylphosphonic acid butyl 4-nitrophenyl ester
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About This Item
Empirical Formula (Hill Notation):
C16H26NO5P
CAS Number:
Molecular Weight:
343.36
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.77
Quality Level
Assay
≥95.0% (HPLC)
storage temp.
−20°C
SMILES string
O=P(OCCCC)(CCCCCC)OC1=CC=C([N+]([O-])=O)C=C1
InChI
1S/C16H26NO5P/c1-3-5-7-8-14-23(20,21-13-6-4-2)22-16-11-9-15(10-12-16)17(18)19/h9-12H,3-8,13-14H2,1-2H3
InChI key
DNVDUMRDCABCRP-UHFFFAOYSA-N
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Regulatory Information
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G Zandonella et al.
European journal of biochemistry, 262(1), 63-69 (1999-05-07)
Fluorescent triacylglycerol analogs were synthesized as covalent inhibitors of lipase activity. The respective 1(3), 2-O-dialkylglycero-3(1)-alkyl-phosphonic acid p-nitrophenyl esters contain a fluorescent pyrenealkyl chain and a long-chain alkyl residue bound to the sn-2 and sn-1(3) positions of glycerol, respectively. The phosphonic
Racemase activity of B. cepacia lipase leads to dual-function asymmetric dynamic kinetic resolution of α-aminonitriles.
Pornrapee Vongvilai et al.
Angewandte Chemie (International ed. in English), 50(29), 6592-6595 (2011-06-03)
Nobuhiko Tokuriki et al.
Nature communications, 3, 1257-1257 (2012-12-06)
Optimization processes, such as evolution, are constrained by diminishing returns-the closer the optimum, the smaller the benefit per mutation, and by tradeoffs-improvement of one property at the cost of others. However, the magnitude and molecular basis of these parameters, and
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