Silane, trimethyl((2-methyl-1-propenyl)oxy)-
Silane, trimethyl((2-methyl-1-propenyl)oxy)- structure
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Common Name | Silane, trimethyl((2-methyl-1-propenyl)oxy)- | ||
|---|---|---|---|---|
| CAS Number | 6651-34-9 | Molecular Weight | 144.287 | |
| Density | 0.8±0.1 g/cm3 | Boiling Point | 119.3±8.0 °C at 760 mmHg | |
| Molecular Formula | C7H16OSi | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | 15.6±8.3 °C | |
| Symbol |
GHS02, GHS07 |
Signal Word | Danger | |
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Preparation of modified peptides: direct conversion of α-amino acids into β-amino aldehydes.
Org. Biomol. Chem. 10(22) , 4448-61, (2012) A direct method for the transformation of α-amino acids into β-amino aldehydes was developed, and applied to the modification of the C-terminal residue of peptides. The method takes place in good yields and under mild conditions. The application of this metho... |
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Induction of the SOS function sfiA in E. coli by systems which generate triplet ketones.
Mutat. Res. 198(1) , 53-60, (1988) Generation of triplet ketones, either chemically through thermal decomposition of 3-hydroxymethyl-3,4,4-trimethyl-1,2-dioxetane and 3-[N-(pyridino)carbamoyl]methyl-3,4,4-trimethyl-1,2-dioxetane++ + or enzymatically via the aerobic oxidation of isobutyraldehyd... |
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Generation of electronically excited triplet species at the cellular level: a potential source of genotoxicity.
Toxicol. Lett. 67(1-3) , 17-28, (1993) Selected enzymatic systems can efficiently produce a product in the electronically excited triplet state. Earlier, only the formation of electronically excited singlet species was known. The formation of triplet species has been demonstrated with both normal ... |