N-Hydroxypiperidine structure
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Common Name | N-Hydroxypiperidine | ||
|---|---|---|---|---|
| CAS Number | 4801-58-5 | Molecular Weight | 101.14700 | |
| Density | 1.07g/cm3 | Boiling Point | 175.7ºC at 760 mmHg | |
| Molecular Formula | C5H11NO | Melting Point | 37-39ºC | |
| MSDS | Chinese USA | Flash Point | 78ºC | |
| Name | 1-Hydroxypiperidine |
|---|---|
| Synonym | More Synonyms |
| Density | 1.07g/cm3 |
|---|---|
| Boiling Point | 175.7ºC at 760 mmHg |
| Melting Point | 37-39ºC |
| Molecular Formula | C5H11NO |
| Molecular Weight | 101.14700 |
| Flash Point | 78ºC |
| Exact Mass | 101.08400 |
| PSA | 23.47000 |
| LogP | 0.79940 |
| Index of Refraction | 1.508 |
| InChIKey | LKPFBGKZCCBZDK-UHFFFAOYSA-N |
| SMILES | ON1CCCCC1 |
| Storage condition | 2~8°C |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3.0 |
| RTECS | TN6829550 |
| HS Code | 2933399090 |
| Precursor 9 | |
|---|---|
| DownStream 3 | |
| HS Code | 2933399090 |
|---|---|
| Summary | 2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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Piperidinols that show anti-tubercular activity as inhibitors of arylamine N-acetyltransferase: an essential enzyme for mycobacterial survival inside macrophages.
PLoS ONE 7(12) , e52790, (2012) Latent M. tuberculosis infection presents one of the major obstacles in the global eradication of tuberculosis (TB). Cholesterol plays a critical role in the persistence of M. tuberculosis within the ... |
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Biological N-oxidation of piperidine in vitro.
Zhongguo Yao Li Xue Bao 10(3) , 252-6, (1989) The biological N-oxidation of piperidine, a pharmacologically active biogenic amine of mammals and human beings, was studied in vitro. After incubation of piperidine-HCl in a fortified rat liver micro... |
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On the effect of thalidomide on Mycobacterium avium subspecies paratuberculosis in culture.
Int. J. Infect. Dis. 13(5) , e254-63, (2009) Without known mechanisms of action, thalidomide is used to treat a variety of non-malignant 'idiopathic' diseases. There is increasing concern that Mycobacterium avium subspecies paratuberculosis (MAP... |
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Name: Compound was evaluated for ability to enhance the binding of (+/-)-[3H]nicotine to th...
Source: ChEMBL
Target: Neuronal acetylcholine receptor subunit alpha-7
External Id: CHEMBL634005
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Name: Ability to enhance the binding of (+/-)-[3H]nicotine to the rat brain P2 fraction at ...
Source: ChEMBL
Target: Neuronal acetylcholine receptor subunit alpha-7
External Id: CHEMBL632853
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Name: Ability to enhance the binding of (+/-)-[3H]nicotine to the rat brain P2 fraction at ...
Source: ChEMBL
Target: Neuronal acetylcholine receptor subunit alpha-7
External Id: CHEMBL636099
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Name: Maximum percent of enhancement of binding.
Source: ChEMBL
Target: Neuronal acetylcholine receptor subunit alpha-7
External Id: CHEMBL874428
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Name: Maximum percent of inhibition of binding was determined
Source: ChEMBL
Target: Neuronal acetylcholine receptor subunit alpha-7
External Id: CHEMBL633999
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Name: Compounds was evaluate for their ability to enhance (+/-)-[3H]nicotine binding at a d...
Source: ChEMBL
Target: Neuronal acetylcholine receptor subunit alpha-7
External Id: CHEMBL638617
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| 1-HYDROXYPIPERIDINE |
| EINECS 225-362-9 |
| MFCD00038048 |
| Piperidin-1-ol |