2,4,6-Trichlorobenzoyl chloride
2,4,6-Trichlorobenzoyl chloride structure
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Common Name | 2,4,6-Trichlorobenzoyl chloride | ||
|---|---|---|---|---|
| CAS Number | 4136-95-2 | Molecular Weight | 243.902 | |
| Density | 1.6±0.1 g/cm3 | Boiling Point | 284.2±35.0 °C at 760 mmHg | |
| Molecular Formula | C7H2Cl4O | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | 118.5±26.5 °C | |
| Symbol |
GHS05 |
Signal Word | Danger | |
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Novel synthetic method for the preparation of amphiphilic hyaluronan by means of aliphatic aromatic anhydrides.
Carbohydr. Polym. 111 , 883-91, (2014) The present work describes a novel and efficient method of synthesis of amphiphilic hyaluronan (HA) by esterification with alkyl fatty acids. These derivatives were synthesized under mild aqueous and well controlled conditions using mixed aliphatic aromatic a... |
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Asymmetric total synthesis of spongistatins 1 and 2.
J. Am. Chem. Soc. 124(20) , 5661-63, (2002) The total synthesis of spongistatin 1 (1) and spongistatin 2 (2) has been achieved through an advanced-stage intermediate. The synthesis is highlighted by a highly convergent assembly of the four key fragments (the C1-C15 AB fragment 2, the C16-C28 CD fragmen... |
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Synthesis of γ- and δ-lactone natural products by employing a trans-cis isomerization/lactonization strategy.
Chem. Pharm. Bull. 61(4) , 464-70, (2013) Alkaline hydrolysis of 4-hydroxy- or/and 5-hydroxy-(2E)-alkenoate followed by acid treatment gave the corresponding (2E)-alkenoic acids which were subjected to lactone formation reaction without further purification. The crude acids were treated with 2,4,6-tr... |
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Fieser, M.
Reagents for Organic Synthesis New York 16 , 353, (1992)
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Improved preparation of angelate esters. Hartmann B, et al.
Tetrahedron Lett. 32(38) , 5077-80, (1991)
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