4-Iodobenzaldehyde structure
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Common Name | 4-Iodobenzaldehyde | ||
|---|---|---|---|---|
| CAS Number | 15164-44-0 | Molecular Weight | 232.02 | |
| Density | 1.9±0.1 g/cm3 | Boiling Point | 264.8±23.0 °C at 760 mmHg | |
| Molecular Formula | C7H5IO | Melting Point | 78-82 °C(lit.) | |
| MSDS | USA | Flash Point | 114.0±22.6 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
Use of 4-Iodobenzaldehyde4-Iodobenzaldehyde is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
| Name | 4-Iodobenzaldehyde |
|---|---|
| Synonym | More Synonyms |
| Description | 4-Iodobenzaldehyde is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
|---|---|
| Related Catalog |
| Density | 1.9±0.1 g/cm3 |
|---|---|
| Boiling Point | 264.8±23.0 °C at 760 mmHg |
| Melting Point | 78-82 °C(lit.) |
| Molecular Formula | C7H5IO |
| Molecular Weight | 232.02 |
| Flash Point | 114.0±22.6 °C |
| Exact Mass | 231.938507 |
| PSA | 17.07000 |
| LogP | 2.83 |
| Vapour Pressure | 0.0±0.5 mmHg at 25°C |
| Index of Refraction | 1.668 |
| Storage condition | Keep Cold |
| Symbol |
GHS07 |
|---|---|
| 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 | R36/37/38 |
| Safety Phrases | S26-S36 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| HS Code | 2913000090 |
| Precursor 9 | |
|---|---|
| DownStream 10 | |
| HS Code | 2913000090 |
|---|---|
| Summary | HS: 2913000090 halogenated, sulphonated, nitrated or nitrosated derivatives of products of heading 2912 Educational tariff:17.0% Tax rebate rate:9.0% Regulatory conditions:none Most favored nation tariff:5.5% General tariff:30.0% |
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Growth of Thin, Anisotropic, π-Conjugated Molecular Films by Stepwise "Click" Assembly of Molecular Building Blocks: Characterizing Reaction Yield, Surface Coverage, and Film Thickness versus Addition Step Number.
J. Am. Chem. Soc. 137 , 8819-28, (2015) We report the systematic characterization of anisotropic, π-conjugated oligophenyleneimine (OPI) films synthesized using stepwise imine condensation, or "click" chemistry. Film synthesis began with a ... |
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Selective cleavage of the carbon-halide bond in substituted benzaldimine monolayers by synchrotron soft X-ray: Anomalously large cleavage rate of the carbon-bromide bond. Moon JH, et al.
Langmuir 16(6) , 2981-84, (2000)
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Trans-Substituted porphyrin building blocks bearing iodo and ethynyl groups for applications in bioorganic and materials chemistry. Ravikanth M, et al.
Tetrahedron 54(27) , 7721-34, (1998)
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| Benzaldehyde, 4-iodo- |
| p-Iodobenzaldehyde |
| VHR DI |
| MFCD00039576 |
| 4-Iodobenzaldehyde |