InChI
1S/C6H13Cl2OP/c1-2-3-4-5-6-10(7,8)9/h2-6H2,1H3
SMILES string
CCCCCCP(Cl)(Cl)=O
InChI key
GZXBQDURAKBNAZ-UHFFFAOYSA-N
assay
95%
form
liquid
refractive index
n20/D 1.465 (lit.)
bp
114-121 °C/16 mmHg (lit.)
density
1.185 g/mL at 25 °C (lit.)
functional group
phosphine oxide
Quality Level
Application
Hexylphosphonic dichloride was used in preparation of:
- hexylphosphonic acid via reaction with water
- phosphonate esters
- methyl 4-methylumbelliferyl hexylphosphonate
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Active-site titration analysis of surface influences on immobilized< i> Candida antarctica</i> lipase B activity.
Laszlo JA, et al.
Journal of Molecular Catalysis. B, Enzymatic, 69(1), 60-65 (2011)
Mechanisms of the shape evolution of CdSe nanocrystals.
Peng ZA and Peng X.
Journal of the American Chemical Society, 123(7), 1389-1395 (2001)
Alessandra Mezzetti et al.
Chemistry & biology, 12(4), 427-437 (2005-04-27)
Synthetic chemists often exploit the high enantioselectivity of lipases to prepare pure enantiomers of primary alcohols, but the molecular basis for this enantioselectivity is unknown. The crystal structures of two phosphonate transition-state analogs bound to Burkholderia cepacia lipase reveal this
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