3-Bromopropan-1-ol
3-Bromopropan-1-ol structure
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Common Name | 3-Bromopropan-1-ol | ||
|---|---|---|---|---|
| CAS Number | 627-18-9 | Molecular Weight | 138.99 | |
| Density | 1.6±0.1 g/cm3 | Boiling Point | 175.3±0.0 °C at 760 mmHg | |
| Molecular Formula | C3H7BrO | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | 93.9±0.0 °C | |
| Symbol |
GHS05, GHS07 |
Signal Word | Danger | |
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Halogenated derivatives QSAR model using spectral moments to predict haloacetic acids (HAA) mutagenicity.
Bioorg. Med. Chem. 16 , 5720-32, (2008) The risk of the presence of haloacetic acids in drinking water as chlorination by-products and the shortage of experimental mutagenicity data for most of them requires a research work. This paper describes a QSAR model to predict direct mutagenicity for these... |
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Chloride-sensitive fluorescent indicators.
Anal. Biochem. 293(1) , 60-6, (2001) Three fluorescent halide-sensitive quinolinium dyes have been produced by the reaction of the 6-methylquinoline heterocyclic nitrogen base with methyl bromide, methyl iodide, and 3-bromo-1-propanol. The quaternary salts, unlike the precursor molecule, are rea... |
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Stereochemical diversity in asymmetric cyclization via memory of chirality.
J. Am. Chem. Soc. 128 , 15394, (2006) An enantiodivergent asymmetric cyclization of N-Boc-N-omega-bromoalkyl-alpha-amino acid derivatives has been developed. With potassium amide bases in DMF, cyclization proceeds with retention of configuration, while inversion of configuration was observed with... |
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Synthesis of molten salt-type polymer brush and effect of brush structure on the ionic conductivity. Yoshizawa M and Ohno H.
Electrochim. Acta 46(10) , 1723-28, (2001)
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Use of self-assembled surfactant systems as media for a substitution reaction.
J. Colloid. Interface Sci. 277(1) , 230-4, (2004) The reaction between 3-bromo-1-propanol and phenol and a series of phenols carrying substituents in 4-position was studied in micellar media and in microemulsions based on either a cationic or a nonionic surfactant. The reactivity and the yield were evaluated... |