1,4-Naphthalenedione,2-bromo- structure
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Common Name | 1,4-Naphthalenedione,2-bromo- | ||
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CAS Number | 2065-37-4 | Molecular Weight | 237.04900 | |
Density | 1.757g/cm3 | Boiling Point | 324.2ºC at 760mmHg | |
Molecular Formula | C10H5BrO2 | Melting Point | 131-133ºC(lit.) | |
MSDS | Chinese USA | Flash Point | 124.7ºC | |
Symbol |
GHS07 |
Signal Word | Warning |
Name | 2-bromonaphthalene-1,4-dione |
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Synonym | More Synonyms |
Density | 1.757g/cm3 |
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Boiling Point | 324.2ºC at 760mmHg |
Melting Point | 131-133ºC(lit.) |
Molecular Formula | C10H5BrO2 |
Molecular Weight | 237.04900 |
Flash Point | 124.7ºC |
Exact Mass | 235.94700 |
PSA | 34.14000 |
LogP | 2.34440 |
Vapour Pressure | 0.00025mmHg at 25°C |
Index of Refraction | 1.674 |
Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xi: Irritant; |
Risk Phrases | 36/37/38 |
Safety Phrases | 26-36 |
RIDADR | NONH for all modes of transport |
HS Code | 2914700090 |
HS Code | 2914700090 |
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Summary | HS: 2914700090 halogenated, sulphonated, nitrated or nitrosated derivatives of ketones and quinones, whether or not with other oxygen function Tax rebate rate:9.0% Supervision conditions:none VAT:17.0% MFN tariff:5.5% General tariff:30.0% |
Potent naphthoquinones against antimony-sensitive and -resistant Leishmania parasites: synthesis of novel α- and nor-α-lapachone-based 1,2,3-triazoles by copper-catalyzed azide-alkyne cycloaddition.
Eur. J. Med. Chem. 63 , 523-30, (2013) Continuing our screening program for novel anti-parasite compounds, we synthesized seven 1,4-naphthoquinones coupled to 1,2,3-triazoles, five nor-β-lapachone-based 1,2,3-triazoles and ten α-lapachone-... |
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2-Bromo-1,4-naphthoquinone: a potentially improved substitute of menadione in Apatone™ therapy.
Braz. J. Med. Biol. Res. 45(8) , 701-10, (2012) Apatone™, a combination of menadione (2-methyl-1,4-naphthoquinone, VK3) and ascorbic acid (vitamin C, VC) is a new strategy for cancer treatment. Part of its effect on tumor cells is related to the ce... |
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Expedient, one-pot preparation of fused indoles via CAN-catalyzed three-component domino sequences and their transformation into polyheterocyclic compounds containing pyrrolo[1,2-a]azepine fragments.
Org. Biomol. Chem. 8(15) , 3426-36, (2010) The CAN-catalyzed three-component between reaction between primary amines, beta-dicarbonyl compounds and naphthoquinones or 2-bromonaphthoquinones afforded, respectively, 5-hydroxybenzo[g]indoles and ... |
MFCD00629301 |
2-bromo-1,4-naphtoquinone |
2-bromonaphthoquinone |
3-Bromo-1,4-naphthoquinone |
2-bromo-naphthalene-1,4-dione |
2-Bromo-1,4-naphthoquinone |