IUPAC/Chemical Name
(4-ethoxyphenyl)(3-(4-fluoro-3-phenoxyphenyl)propyl)dimethylsilane
InChi Key
HPYNBECUCCGGPA-UHFFFAOYSA-N
InChi Code
InChI=1S/C25H29FO2Si/c1-4-27-21-13-15-23(16-14-21)29(2,3)18-8-9-20-12-17-24(26)25(19-20)28-22-10-6-5-7-11-22/h5-7,10-17,19H,4,8-9,18H2,1-3H3
SMILES Code
CCOc1ccc([Si](C)(CCCc2cc(Oc3ccccc3)c(F)cc2)C)cc1
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>3 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
Preparing Stock Solutions
The following data is based on the
product
molecular weight
408.59
Batch specific molecular weights may vary
from batch to batch
due to the degree of hydration, which will
affect the solvent
volumes required to prepare stock solutions.
| Concentration / Solvent Volume / Mass |
1 mg |
5 mg |
10 mg |
| 1 mM |
1.15 mL |
5.76 mL |
11.51 mL |
| 5 mM |
0.23 mL |
1.15 mL |
2.3 mL |
| 10 mM |
0.12 mL |
0.58 mL |
1.15 mL |
| 50 mM |
0.02 mL |
0.12 mL |
0.23 mL |
1: Peng D, Zhang Y, Du X, Zhang L, Leng X, Walter MD, Huang Z. Phosphinite- iminopyridine iron catalysts for chemoselective alkene hydrosilylation. J Am Chem Soc. 2013 Dec 26;135(51):19154-66. doi: 10.1021/ja404963f. Epub 2013 Dec 13. PMID: 24304467.
2: Inubushi H, Kondo H, Lesbani A, Miyachi M, Yamanoi Y, Nishihara H. Direct synthesis of alkylsilanes by platinum-catalyzed coupling of hydrosilanes and iodoalkanes. Chem Commun (Camb). 2013 Jan 7;49(2):134-6. doi: 10.1039/c2cc35150a. PMID: 23072826.
3: Takeuchi H, Endo N. Insecticide susceptibility of Nezara viridula (Heteroptera: Pentatomidae) and three other stink bug species composing a soybean pest complex in Japan. J Econ Entomol. 2012 Jun;105(3):1024-33. doi: 10.1603/ec11383. PMID: 22812144.
4: Katsuda Y, Minamite Y, Vongkaluang C. Development of Silafluofen-Based Termiticides in Japan and Thailand. Insects. 2011 Dec 8;2(4):532-9. doi: 10.3390/insects2040532. PMID: 26467832; PMCID: PMC4553446.
5: Tisch M, Faulde M, Maier H. Genotoxische Effekte aktuell gebräuchlicher Insektizide auf humane Tonsillenschleimhautepithelien [Genotoxic effects of insecticides in current use on mucosal epithelial cells from human tonsil tissue]. HNO. 2007 May;55 Suppl 1:E15-22. German. doi: 10.1007/s00106-006-1481-9. PMID: 17149631.
6: Goto S, Asada S, Fushiwaki Y, Mori Y, Tanaka N, Umeda M, Nakajima D, Takeda K. Tumor-promoting activity and mutagenicity of 5 termiticide compounds. J UOEH. 2004 Dec 1;26(4):423-30. doi: 10.7888/juoeh.26.423. PMID: 15624354.
7: Satoh M, Sakaguchi M, Kobata M, Sakaguchi Y, Tanizawa H, Miura Y, Sasano R, Nakanishi Y. [Effects of rice cleaning and cooking process on the residues of flutolanil, fenobucarb, silafluofen and buprofezin in rice]. Shokuhin Eiseigaku Zasshi. 2003 Feb;44(1):7-12. Japanese. doi: 10.3358/shokueishi.44.7. PMID: 12749190.
8: Nakata M, Fukushima A, Ohkawa H. A monoclonal antibody-based ELISA for the analysis of the insecticide flucythrinate in environmental and crop samples. Pest Manag Sci. 2001 Mar;57(3):269-77. doi: 10.1002/ps.286. PMID: 11455657.
