MM 47755
Modify Date: 2024-01-03 12:48:52
MM 47755 structure
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Common Name | MM 47755 | ||
|---|---|---|---|---|
| CAS Number | 117620-87-8 | Molecular Weight | 336.33800 | |
| Density | 1.39g/cm3 | Boiling Point | 583.3ºC at 760mmHg | |
| Molecular Formula | C20H16O5 | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | 214.3ºC | |
| Symbol |
GHS07, GHS09 |
Signal Word | Warning | |
Use of MM 47755MM 47755 is a new benz[a]anthracene antibiotic from a streptomycete. |
| Name | 3-hydroxy-8-methoxy-3-methyl-2,4-dihydrobenzo[a]anthracene-1,7,12-trione |
|---|---|
| Synonym | More Synonyms |
| Density | 1.39g/cm3 |
|---|---|
| Boiling Point | 583.3ºC at 760mmHg |
| Molecular Formula | C20H16O5 |
| Molecular Weight | 336.33800 |
| Flash Point | 214.3ºC |
| Exact Mass | 336.10000 |
| PSA | 80.67000 |
| LogP | 2.35050 |
| Vapour Pressure | 1.89E-14mmHg at 25°C |
| Index of Refraction | 1.652 |
| Symbol |
GHS07, GHS09 |
|---|---|
| Signal Word | Warning |
| Hazard Statements | H302-H410 |
| Precautionary Statements | P273-P501 |
| RIDADR | UN 3077 9 / PGIII |
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Angucyclinone antibiotics: total syntheses of YM-181741, (+)-ochromycinone, (+)-rubiginone B2, (-)-tetrangomycin, and MM-47755.
J. Org. Chem. 72(16) , 6116-26, (2007) A concise and highly enantioselective route has been developed for the synthesis of angucyclinone-type natural products. Utilizing this strategy, total syntheses of five natural products YM-181741, (+... |
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Total synthesis of (-)-8-O-methyltetrangomycin (MM 47755).
Org. Lett. 8(12) , 2507-10, (2006) A stereoselective total synthesis of the natural antibiotic (-)-8-O-methyltetrangomycin 1 is reported. The essential steps for this convergent synthesis are the transformation of a geraniol epoxide in... |
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The cobalt way to angucyclinones: asymmetric total synthesis of the antibiotics (+)-rubiginone B2, (-)-tetrangomycin, and (-)-8-O-methyltetrangomycin.
Chemistry 16(29) , 8805-21, (2010) A cobalt(I)-mediated convergent and asymmetric total synthesis of angucyclinones with an aromatic B ring has been developed. In the course of our research, we synthesized three naturally occurring ang... |
| 6-Deoxy-8-O-methylrabelomycin |