![]() triisopropyl phosphate structure
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Common Name | triisopropyl phosphate | ||
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CAS Number | 513-02-0 | Molecular Weight | 224.23400 | |
Density | 1.012g/cm3 | Boiling Point | 222.2ºC at 760mmHg | |
Molecular Formula | C9H21O4P | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | 102.4ºC | |
Symbol |
![]() ![]() ![]() GHS02, GHS07, GHS09 |
Signal Word | Warning |
Fungal recognition enhances mannose receptor shedding through dectin-1 engagement.
J. Biol. Chem. 286(10) , 7822-9, (2011) The mannose receptor (MR) is an endocytic type I membrane molecule with a broad ligand specificity that is involved in both hemostasis and pathogen recognition. Membrane-anchored MR is cleaved by a metalloproteinase into functional soluble MR (sMR) composed o... |
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The effect of triisopropyl phosphate on the mobility of surface concanavalin A receptors and on the locomotion of polymorphonuclear leucocytes.
Exp. Cell Res. 94(2) , 292-8, (1975)
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Efficient and ‘green’microwave-assisted synthesis of haloalkylphosphonates via the Michaelis–Arbuzov reaction. Jansa P, et al.
Green Chem. 13(4) , 882-888, (2011)
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Reactions of Trialkyl Phosphates, Alkyl Acetates, and Tertiary Butyl Hypochlorite in the Friedel-Crafts Syntheses1. Berman N and Lowy A.
J. Am. Chem. Soc. 60(11) , 2596-2597, (1938)
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Dealkylation and debenzylation of triesters of phosphoric acid. Phosphorylation of hydroxy and amino compounds. Zervas L and Dilaris I.
J. Am. Chem. Soc. 77(20) , 5354-5357, (1955)
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Carbonium ion formation in solvolysis of phosphate triesters. Cox Jr JR and Newton MG.
J. Org. Chem. 34(9) , 2600-2605, (1969)
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