6-Bromindan-1-on structure
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Common Name | 6-Bromindan-1-on | ||
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CAS Number | 1775-27-5 | Molecular Weight | 211.055 | |
Density | 1.6±0.1 g/cm3 | Boiling Point | 283.9±29.0 °C at 760 mmHg | |
Molecular Formula | C9H7BrO | Melting Point | 39-44 °C | |
MSDS | Chinese USA | Flash Point | 106.1±11.6 °C | |
Symbol |
GHS05 |
Signal Word | Danger |
Name | 2-Bromo-1-indanone |
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Synonym | More Synonyms |
Density | 1.6±0.1 g/cm3 |
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Boiling Point | 283.9±29.0 °C at 760 mmHg |
Melting Point | 39-44 °C |
Molecular Formula | C9H7BrO |
Molecular Weight | 211.055 |
Flash Point | 106.1±11.6 °C |
Exact Mass | 209.968018 |
PSA | 17.07000 |
LogP | 2.45 |
Vapour Pressure | 0.0±0.6 mmHg at 25°C |
Index of Refraction | 1.635 |
Symbol |
GHS05 |
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Signal Word | Danger |
Hazard Statements | H314 |
Precautionary Statements | P280-P305 + P351 + P338-P310 |
Personal Protective Equipment | Eyeshields;Faceshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges |
Hazard Codes | C:Corrosive; |
Risk Phrases | R34 |
Safety Phrases | S24/25-S36/37/39-S27-S26 |
RIDADR | UN 1759 |
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% |
Purification and characterization of NADPH-dependent aldo-keto reductase specific for beta-keto esters from Penicillium citrinum, and production of methyl (S)-4-bromo-3-hydroxybutyrate.
Appl. Microbiol. Biotechnol. 66(1) , 53-62, (2004) A novel beta-keto ester reductase (KER) was purified to homogeneity from recombinant Escherichia coli (pTrcKER) cells, which efficiently expressed the ker gene cloned from Penicillium citrinum IFO4631... |
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Expoxy ketones. VII. The stereochemistry of spiroepoxy ketones. Reactions of 2-benzal-1-indanone oxide. Cromwell NH and Martin JL.
J. Org. Chem. 33(5) , 1890-94, (1968)
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The synthesis of derivatives of 1-indanone and indenone. House HO, et al.
J. Am. Chem. Soc. 82(6) , 1452-7, (1960)
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6-Bromindan-1-on |
1-Indanone, 6-bromo- |
6-Bromo-2,3-dihydro-1H-inden-1-one |
MFCD00041030 |
2-bromo-2,3-dihydroinden-1-one |
2-Bromoindanone,tech. |
1H-Inden-1-one, 6-bromo-2,3-dihydro- |
6-Brom-2,3-dihydro-1H-inden-1-on |
2-Bromoindan-1-one |
6-bromoindan-1-one |
2-Brom-2,3-dihydro-1H-inden-1-on |
2-bromoindanone |
1H-Inden-1-one, 2-bromo-2,3-dihydro- |
2-BroMo-1-indanone,tech.,8 |
L56 BVT&J HE |
6-Bromo-1-indanone |
2-Bromo-1-indanone |
2-bromo-2,3-dihydro-1H-inden-1-one |
6-Bromo-indan-1-one |
2-BROMO-1-INDANONE: TECH. |