1H-Isoindole-1,3(2H)-dione,5,6-dichloro-
1H-Isoindole-1,3(2H)-dione,5,6-dichloro- structure
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Common Name | 1H-Isoindole-1,3(2H)-dione,5,6-dichloro- | ||
|---|---|---|---|---|
| CAS Number | 15997-89-4 | Molecular Weight | 216.02100 | |
| Density | 1.643g/cm3 | Boiling Point | N/A | |
| Molecular Formula | C8H3Cl2NO2 | Melting Point | 217-219ºC(lit.) | |
| MSDS | Chinese USA | Flash Point | N/A | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Phosphine-catalyzed allylic substitution of Morita-Baylis-Hillman acetates: synthesis of N-protected beta-aminophosphonic acid esters.
J. Org. Chem. 71(20) , 7892-7894, (2006) A series of N-protected beta-amino phosphonic acid esters have been prepared by phosphine-catalyzed allylic substitution of 2-(diethylphosphonyl)-substituted allylic acetates employing 4,5-dichlorophthalimide as nucleophilic partner. These organocatalytic all... |
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Synthesis and antiviral activity of some 5'-N-phthaloyl-3'-azido-2',3'-dideoxythymidine analogues.
Antivir. Chem. Chemother. 14(3) , 139-144, (2003) A variety of substituted 5'-N-phthaloyl-3'-azido-2',3'-dideoxythymidine derivatives has been evaluated for their activity against HIV-1, HIV-2 and Moloney murine sarcoma virus (MSV) in cell culture. Most of the 3'-azido-2',3'-dideoxythymidine (AZT, zidovudine... |
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Synthesis of water soluble PEGylated (copper) phthalocyanines via Mitsunobu reaction and Cu (i)-catalysed azide-alkyne cycloaddition (CuAAC) click chemistry. Li M, et al.
Polym. Chem. 4(16) , 4405-4411, (2013)
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Additive effects in Ir-BICP catalyzed asymmetric hydrogenation of imines. Zhu G and Zhang X.
Tetrahedron Asymmetry 9(14) , 2415-2418, (1998)
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Convenient synthesis of phthalocyanines with disilazanes under mild conditions. Uchida H, et al.
ARKIVOC 11 , 17-23, (2005)
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I-Line Sensitive Photoacid Generators Having Thianthrene Skeleton. Okamura H, et al.
J. Photopolym. Sci. Technol. 17(1) , 131-134, (2004)
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Conversion of phthalimides to isoindolines by diborane. 8 Strassert CA and Awruch J.
Monatsh. Chem 137(12) , 1499-1503, (2006)
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Polarizability and first-order hyperpolarizability of cyclic imides. Asghari-Khiavi M, et al.
J. Mol. Struct. (Theochem) 910(1) , 56-60, (2009)
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