6-Chloro-1H-indole
6-Chloro-1H-indole structure
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Common Name | 6-Chloro-1H-indole | ||
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| CAS Number | 17422-33-2 | Molecular Weight | 151.59 | |
| Density | 1.3±0.1 g/cm3 | Boiling Point | 293.0±13.0 °C at 760 mmHg | |
| Molecular Formula | C8H6ClN | Melting Point | 87-90 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 158.9±5.4 °C | |
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Design, synthesis and structure-activity relationship studies of novel and diverse cyclooxygenase-2 inhibitors as anti-inflammatory drugs.
J. Enzyme Inhib. Med. Chem. 29(6) , 846-67, (2014) Because of the pivotal role of cyclooxygenase (COX) in the inflammatory processes, non-steroidal anti-inflammatory drugs (NSAIDs) that suppress COX activities have been used clinically for the treatment of inflammatory diseases/syndromes; however, traditional... |
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Toward prediction of alkane/water partition coefficients.
J. Med. Chem. 51 , 3720-30, (2008) Partition coefficients were measured for 47 compounds in the hexadecane/water ( P hxd) and 1-octanol/water ( P oct) systems. Some types of hydrogen bond acceptor presented by these compounds to the partitioning systems are not well represented in the literatu... |
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Production of substituted L-tryptophans by fermentation.
Appl. Microbiol. 21(5) , 841-3, (1971) Claviceps purpurea has been shown to produce extracellular l-tryptophan from indole in stirred fermentors. The substrate specificity of this conversion was investigated by using substituted indoles, anthranilic acid, and 4-chloro-anthranilic acid. Addition of... |