9-Fluorenone Hydrazone structure
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Common Name | 9-Fluorenone Hydrazone | ||
|---|---|---|---|---|
| CAS Number | 13629-22-6 | Molecular Weight | 194.23200 | |
| Density | 1.23 g/cm3 | Boiling Point | 362.5ºC at 760 mmHg | |
| Molecular Formula | C13H10N2 | Melting Point | 148-150 °C(lit.) | |
| MSDS | N/A | Flash Point | 173ºC | |
| Name | 9-Fluorenone Hydrazone |
|---|---|
| Synonym | More Synonyms |
| Density | 1.23 g/cm3 |
|---|---|
| Boiling Point | 362.5ºC at 760 mmHg |
| Melting Point | 148-150 °C(lit.) |
| Molecular Formula | C13H10N2 |
| Molecular Weight | 194.23200 |
| Flash Point | 173ºC |
| Exact Mass | 194.08400 |
| PSA | 38.38000 |
| LogP | 3.07840 |
| Vapour Pressure | 1.93E-05mmHg at 25°C |
| Index of Refraction | 1.682 |
| InChIKey | YCNUILAKOMIBAL-UHFFFAOYSA-N |
| SMILES | NN=C1c2ccccc2-c2ccccc21 |
| Hazard Codes | Xi: Irritant; |
|---|---|
| Risk Phrases | R36/37/38 |
| Safety Phrases | S26-S36 |
| WGK Germany | 3 |
| HS Code | 2928000090 |
| Precursor 10 | |
|---|---|
| DownStream 10 | |
| HS Code | 2928000090 |
|---|---|
| Summary | 2928000090 other organic derivatives of hydrazine or of hydroxylamine VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0% |
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Name: Cytotoxicity against human RPMI8226 cells after 48 hrs by MTT assay
Source: ChEMBL
Target: RPMI-8226
External Id: CHEMBL4047135
|
|
Name: Discovery of Small Molecules to Inhibit Human Cytomegalovirus Nuclear Egress
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
Target: HCMV UL50
External Id: HMS1262
|
|
Name: Cytotoxicity against human MM1S cells after 48 hrs by MTT assay
Source: ChEMBL
Target: MM1.S
External Id: CHEMBL4047136
|
|
Name: Screen for inhibitors of RMI FANCM (MM2) intereaction
Source: 11908
Target: N/A
External Id: RMI-FANCM-MM2
|
|
Name: Chemical Probes of Kaposi's Sarcoma Herpes Virus Latent Infection
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
Target: ORF 73 [Human herpesvirus 8 type M]
External Id: HMS791
|
|
Name: Inhibition of mTOR binding to DEPTOR in human RPMI8226 cells assessed as increase in ...
Source: ChEMBL
Target: DEP domain-containing mTOR-interacting protein
External Id: CHEMBL4047134
|
|
Name: A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id: HMS979
|
|
Name: Cytotoxicity in human RPMI8226 cells incubated for 48 hrs by MTT assay
Source: ChEMBL
Target: RPMI-8226
External Id: CHEMBL4418221
|
|
Name: Inhibition of DEPTOR in human RPMI8226 cells assessed as increase in mTOR kinase acti...
Source: ChEMBL
Target: DEP domain-containing mTOR-interacting protein
External Id: CHEMBL4418222
|
|
Name: Cytotoxicity in human MM1S cells incubated for 48 hrs by MTT assay
Source: ChEMBL
Target: MM1.S
External Id: CHEMBL4418223
|
| FLUOREN-9-YLIDENE-HYDRAZINE |
| EINECS 237-116-8 |
| fluoren-9-ylidenehydrazine |
| 9-FLUORENONE HYDRAZONE |
| MFCD00016357 |